# FewerJobs export - 100 curated jobs Generated: 2026-06-18T15:17:07.825Z Source: https://fewerjobs.com ## Filters applied - **q**: Bicara Therapeutics Inc - **quality_floor**: default - **match_401k_strict**: true - **parental_strict**: true - **non_birth_strict**: true - **pto_strict**: true - **include_older**: false - **apply_url_verified**: false - **page**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Senior Medical Science Liaison (multiple territories) - Bicara Therapeutics Inc - Location: United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-21 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/b1da34cf-7830-446c-b4bc-63b2dbf0f251 - Excerpt: Senior Medical Science Liaison (multiple territories) United States Position Overview The Senior Medical Science Liaison (MSL) role is the field-based medical/scientific expert for the company, focusing on engagement with healthcare providers to provide fair/balanced education on investigational products, understanding the evolving therapeutic landscape, and supporting research collaborations across the portfolio. We are building our Field Medical team and are open to hiring in multiple territories for qualified candidates. Responsibilities - Identifies, establishes, and maintains collaborative relationships with key investigators, institutions, groups and consortia in disease state areas of strategic focus for the company. - Provides education to the medical community on the company's investigational products and disease areas of focus. - Increases company visibility and enhances professional interaction with current and future oncology leaders. - Participates in medical education for healthcare professionals, including formulary (P&T) committees, through presentations at appropriate venues. - Works with the appropriate departments/personnel at clinical sites to ensure required education and training are provided as needed. - Identifies clinical research opportunities that are consistent with company objectives. - Is the primary territory contact for the investigator-initiated research program, facilitating the process from concept submission through publication. - Identifies and communicates key clinical and research insights from oncology leaders to help shape company research. - Maintains a high level of clinical and scientific expertise through ongoing training and self-education, including attendance of relevant conferences, scientific workshops, and review of key publications. - Gathers and disseminates competitive intelligence in a compliant manner. - Takes advantage of opportunities to ### Program Manager - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-06 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/7cbf6e46-6687-4ab2-9255-085caa202ed3 - Excerpt: Program Manager Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Program Manager to provide program and project management expertise and operational leadership to the team. The role is highly cross-functional with key interactions with preclinical, clinical, medical, regulatory, and finance. The Program Manager will assist in developing project plans and budgets, identify critical path activities, and manage risks in conjunction with working teams. The successful candidate will have strong communication skills and understand the drug development process. They will be highly organized, detail-oriented, and comfortable with ambiguity. The role will report to the Associate Director, Program Management. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities • Provide program management support for research teams, working groups, and development teams including timelines, budget development, and meeting management. • Develop and maintain integrated project plans, identify key project milestones, document and track actions and decisions, and conduct risk assessments. • Work closely with internal stakeholders to maintain cross-functional oversight and ensure transparency of project status. • Support clear communication with team members and stakeholders, including senior leadership. • Foster a sense of inclusion and create a shared sense of purpose. Qualifications • Bachelor's degree required, preferably in life sciences or a related field. Advanced degree (MS, MBA, PhD) a plus. • 4+ years of industry experience, including at least 1 year of program/project management experience in the biotech/pharmaceutical industry. Preference for experience in oncology drug development. • Proficiency ### Senior Director, Field Medical Affairs & US Launch Lead - Bicara Therapeutics Inc - Location: United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-20 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/743091e6-f0d2-46dd-a08f-207292e5ded9 - Excerpt: Senior Director, Field Medical Affairs & US Launch Lead United States Position Overview Bicara is seeking a strategic and execution-driven Field Medical Affairs Lead to build, lead, and spearhead our field medical organization for medical launch readiness and through our commercial launch. This is a highly visible, cross-functional role that sits at the intersection of science, strategy, and stakeholder engagement. This is a rare opportunity to architect the field medical function from the ground up - defining the MSL model, establishing engagement standards, and leading a high-performing team of Medical Science Liaisons (MSLs) at a pivotal moment in the company's history. The ideal candidate combines strategic vision with hands-on field leadership, bringing deep experience in MSL team management, KOL engagement, and launch execution within biotech or specialty pharma. This role is field based and requires the ability to travel up to 60-70% within assigned territory. Responsibilities Field Organization Leadership - Recruit, onboard, train, and lead a national team of Medical Science Liaisons (MSLs), building a field medical function calibrated for launch readiness. - Define and implement the field medical operating model, including territory design, call planning frameworks, engagement metrics, and performance standards. - Serve as a player-coach, maintaining a personal portfolio of national/academic KOL relationships while guiding the team's strategic engagement plans. - Foster a high-performance, learning-oriented team culture rooted in scientific integrity, compliance, and patient-centricity. Launch Strategy, Readiness & Execution - Co-development and execution of the Medical Affairs Launch Plan with VP Medical affairs, ensuring alignment with commercial, clinical, ### Senior Director, Commercial Packaging, Serialization and Global Logistics - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-01 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/792e24c6-c7f5-4bfa-9142-bea1d7054f96 - Excerpt: Senior Director, Commercial Packaging, Serialization and Global Logistics Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Senior Director of Global Logistics, Commercial Packaging and Serialization that will play a pivotal role in shaping and executing Bicara's global Supply Chain strategy. This role will have immediate impact on establishment and oversight of our commercial packaging and distribution along with strategy and operational oversight of the end-to-end global logistics across both clinical and commercial supply chain. This position reports to the Senior Vice President, Supply Chain and serves as a key member of the leadership team with close partnership and collaboration with Technical Operations, Clinical Supply, Quality, Regulatory, Commercial, Finance, Legal, and a wide range of global external partners across drug substance, drug product, packaging and commercial distribution. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities - Commercial Packaging - Provides strategic leadership, functional oversight and operational oversight during the commercial packager selection process. Oversees the RFP process and packaging partner selection, contracting, qualification and ongoing performance management. - Ensures that packaging design, artwork implementation, and labeling strategies support regulatory & global compliance requirements while meeting Bicara's commercial objectives. - Drives all commercial packaging aspects of the future BLA submission and commercial market launches. - Ensures alignment of all packaging components and processes with regulatory filings, specifically Bicara's first BLA submission, such as compliance of container closure systems, adherence to approved labeling as defined in regulatory submissions ### Senior Director, GxP Quality Management Systems (QMS) - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/4b2b6299-717d-4219-8406-3e3ca467ef82 - Excerpt: Senior Director, GxP Quality Management Systems (QMS) Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Senior Director, Quality Management Systems (QMS), reporting to the VP, Global Quality, to build and lead the company's QMS from the ground up. This hands-on leadership role will establish a scalable, phase-appropriate quality framework that supports all GxP activities while driving speed, operational efficiency, and sustained inspection readiness. As a key member of the Quality leadership team, this individual will partner closely with GMP and GCP Quality leaders to design and implement pragmatic, risk-based processes and a fit-for-purpose operating model. The role is accountable for establishing robust systems, governance, and tools that support effective execution, while preserving the agility required to scale alongside organizational growth across clinical and commercial activities. This role is ideal for a leader who excels in a fast-paced, build-mode environment, balancing strategic vision with hands-on execution. The successful candidate brings a collaborative, solutions-oriented approach to partnering across Quality and cross-functional teams and will embed quality into the company's operating model-fostering accountability, simplicity, and continuous improvement as the organization grows. This role is based in Boston with a hybrid schedule (three days onsite per week); however, a remote schedule may be considered. Responsibilities QMS Leadership - Design, implement, and continuously improve an integrated QMS to support all GxP activities at Bicara - Partner with GMP and GCP Quality leads to build practical, fit-for-purpose processes - Lead the establishment of QMS governance, driving consistent and effective use of quality systems ### Senior Director, IT Business Partner (Commercial, Medical & Patient Engagement) - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-11 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/89bfc901-ad7c-44d8-98d0-43fd9b1ced67 - Excerpt: Senior Director, IT Business Partner (Commercial, Medical & Patient Engagement) Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Senior Director, IT Business Partner (Commercial, Medical & Patient Engagement) to play a pivotal role in shaping and delivering the company's digital strategy across Medical Affairs, Commercial, and Patient-focused functions. This individual will lead the design and execution of a scalable, compliant, and data-driven technology ecosystem that supports medical operations today and enables Commercial launch readiness. Reporting to the VP of IT and partnering closely with the Commercial, Medical Affairs, Market Access, and Patient Advocacy teams, this role is critical in ensuring that Bicara's digital capabilities are aligned with business strategy, regulatory requirements, and long-term growth objectives. This role forms a critical pillar of the IT Leadership Team, playing a central role in shaping and executing Bicara's future digital ecosystem. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities IT Business Partnership & Strategy - Serve as the primary IT partner to Medical Affairs, Commercial, Market Access, and Patient Advocacy teams, ensuring strong alignment between business priorities and technology solutions. - Translate business strategy into a clear, phased digital roadmap spanning Medical through Commercial launch and beyond. - Partner with senior leadership to shape launch readiness strategy, ensuring systems and data decisions are scalable and fit for commercialization. - Contribute to cross-functional planning and provide strategic input into business and operational decisions. - Oversee external vendors, CROs, and ### Director, Medical Writing - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/da7bb5bd-167d-4821-b294-dc2766ecb308 - Excerpt: Director, Medical Writing Boston, MA, United States Position Overview Bicara Therapeutics is seeking a proactive and detail-oriented Director, Medical Writing to lead the development of complex, high-quality scientific documents that support our clinical development and regulatory submissions. Reporting to the VP, Regulatory Affairs, the ideal candidate will work closely with regulatory leadership, cross-functional teams and external partners to deliver accurate, clear, and compliant documentation on time. This role is ideal for an experienced Medical Writer who thrives in a small, fast-moving biotech environment. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities - Lead the Medical Writing efforts and strategy for clinical and strategic regulatory documents, ensuring high quality and on-time writing deliverables in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs). This includes but is not limited to health authority briefing packages, pediatric plans, designation requests, clinical protocols, investigator brochures, clinical study reports, and IND/BLA summary documents. - Document lead for regulatory document creation, review and approval process. - Works with project team members to develop a plan and timelines for regulatory document initiation and completion. - Partner with cross-functional leads to interpret and present nonclinical and/or clinical data in documents for regulatory submission. - Contributes to documents for regulatory submission in accordance with applicable regulatory guidelines. - Coordinates and drives the adjudication of review comments with other authors and reviewers and provides timely follow-up to address outstanding queries or comments until resolution. ### Director, Formulation and Drug Product Development - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-08 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/59b95f6a-bd9e-4890-8be7-ee74e2d29b3f - Excerpt: Director, Formulation and Drug Product Development Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Director, Formulation and Drug Product Development who will lead the formulation and process development for complex biologics, with a strong emphasis on bispecifics, and fusion proteins, progressing into pivotal studies and commercial readiness. This role oversees drug product control strategy, process validation, and BLA/MMA submissions. The ideal candidate will bring expertise in late-stage development and establishment of drug product control strategies for bispecifics and fusion proteins including experience with Liguid/Lyo process development strategies, and high concentration formulation development. Responsibilities - Develop drug product development strategies through internal/external partnerships and product integration into drug/device combination products. - Oversee, scale-up, and characterize drug product manufacturing processes, including sterile filtration, filling/finish processes, and lyophilization - Oversee drug product development activities, ensuring successful tech transfer, characterization, and process validation - Serve as a subject matter expert on high concentration formulation development with experience in, control of aggregation, viscosity, and sub-visible particles - Provide technical guidance during investigations at CMOs/CROs and review technical development documents - Develop regulatory strategies and draft regulatory submissions including INDs, IMPDs, BLAs, and MAAs - 20-25% travel in support of manufacturing and development activities at CDMOs. - Collaborate with cross-functional teams, including analytical development, quality assurance, regulatory affairs, and manufacturing, to ensure seamless integration and success. Qualifications - M.S. with 12+ years or a Ph.D. in biochemical engineering, chemical engineering, biochemistry, or pharmaceutical sciences, with at least 8+ years of experience in an ### Clinical Trial Associate (APAC) - Bicara Therapeutics Inc - Location: Asia-Pacific (APAC), Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-05-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/8b79dd39-5243-4168-9202-ca9fa10d8719 - Excerpt: Clinical Trial Associate (APAC) Asia-Pacific (APAC), Singapore Position Overview The Clinical Trial Associate (CTA) at Bicara Therapeutics plays a critical role on the Clinical Operations team by supporting the planning, execution, and management of clinical trials. The CTA will work closely with Clinical Trial Managers (CTMs) and other cross-functional teams to ensure that trials are conducted efficiently, in compliance with regulatory requirements, and in accordance with the study protocol. This position will report to the APAC Clinical Trial Manager, Clinical Operations. This position is remote, with a strong preference for candidates located within the APAC region. Responsibilities - Assist in the coordination and management of clinical trials, including study start-up, maintenance, and close-out activities in close collaboration with Clinical Trial Managers and CRO. - Support Clinical Trial Managers in overseeing CRO deliverables, timelines, issue escalation, and overall study operational performance across assigned regions and sites. - Proactively identify and escalate operational risks, delays, or quality issues to the Clinical Trial Manager. - Maintain, organize, and update essential study documentation to ensure they are complete, accurate, and audit-ready at all times. - Facilitate effective communication among study sites, Clinical Trial Managers, and other stakeholders by managing correspondence, coordinating meetings, and distributing study-related information, including preparing agendas, tracking action items, documenting decisions, and following up on outstanding deliverables. - Support the site start-up and activation process, including collection and tracking of essential documents in accordance with the EDP; coordination of EC/RA submissions and approvals; vendor coordination; and follow-up with CRO teams to ### Senior Director, GMP Quality Operations & Supplier Quality - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-04-28 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/1e59dd84-6dae-4372-8022-efe024f08846 - Excerpt: Senior Director, GMP Quality Operations & Supplier Quality Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Senior Director, GMP Quality & Supplier Quality to provide leadership and oversight of GMP Quality operations supporting external manufacturing, quality control, packaging and labeling, QP release, and global distribution. This role is critical to ensuring sustained inspection readiness as the organization advances through Phase 3, regulatory submission, and commercialization. The position will initially focus on clinical supply through external partners and will play a key role in building scalable Quality processes to support commercial readiness, including batch disposition, QP release, and global supply oversight. Operating within a matrixed global Quality organization, this role requires a balance of strategic leadership and hands-on execution, with strong cross-functional collaboration across Technical Operations, Quality Systems, and external partners. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities - Provide end-to-end Quality oversight of CDMOs, contract laboratories, and packaging/labeling vendors supporting clinical and future commercial supply. - Lead supplier qualification, performance management, and establishment of robust Quality Agreements. - Ensure effective oversight and timely resolution of deviations, investigations, CAPAs, and change controls across external partners. - Establish and implement scalable, end-to-end batch disposition processes aligned with global regulatory expectations. - Build and operationalize QP release frameworks in collaboration with EU Qualified Persons and external manufacturers. - Partner with Technical Operations and CDMOs to support PPQ readiness and execution, ensuring alignment on Quality expectations. - Contribute ### Senior Manager, Payroll and Equity - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-04-28 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/04518c68-11db-4e36-993b-f9519e9e4eef - Excerpt: Senior Manager, Payroll and Equity Boston, MA, United States Position Overview Bicara Therapeutics is seeking a proactive and detailed-oriented Senior Manager, Payroll and Equity to join our growing Accounting Team. This individual will report to the Director, Accounting and will be responsible for timely and compliant processing for all US multi-state payroll and equity cycles, including semi-monthly payrolls, special/off-cycle payrolls and equity grants as well as partner with cross-functional teams to support global payroll. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities: - Own end-to-end processing for semi-monthly and/or bi-weekly payroll across all U.S. states, including exempt and non-exempt employees. - Prepare and process special payrolls, including stock option exercises. - Maintain compliance with state and local tax registrations, withholding requirements, SUI rates, and year-end filings (W-2, ACA). - Maintain payroll system accuracy, including earnings codes, deductions, tax configurations, and pay rules. - Own year-end payroll activities, including review of forms 3921/3922, W-2, as well as fringe benefit reporting, 401k limits, and ensuring accuracy of state tax rates. - Partner with HR and Finance to ensure accurate new hire setup, terminations, leave of absence pay, equity income, and bonus processing. - Manage multi-state nexus tracking and proactively flag new jurisdictional obligations as headcount expands. - Review and approve monthly EOR invoices; reconcile EOR payroll registers against HR records and Finance cost centers. - Oversee payroll tax filings, payments, corrections, and resolve tax issues. - Review payroll for non-US ### Senior Project Manager, Clinical Operations - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-06 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/1d713013-9aad-4230-9d78-0accfb461335 - Excerpt: Senior Project Manager, Clinical Operations Boston, MA, United States Position Overview Bicara Therapeutics is seeking a Senior Project Manager to provide project management expertise and strong operational support and leadership to the team. The role is highly cross-functional with key interactions with internal and external stakeholders. In partnership with the Clinical Operations Team, the Project Manager will assist in developing integrated plans and will understand developing strategy, identifying critical path activities and determining risks / mitigation plans. The successful candidate will have strong communication skills. They will be highly organized, detail oriented, comfortable with ambiguity, and have a proven track record of managing and driving projects. The role will report to the Senior Director, Clinical Operations. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities - Serve as an integral part of the Clinical Operations core team to drive operations efficiently including generating integrated project plans, identifying and tracking key project milestones and metrics, and monitoring budgets, invoices, and accruals. - Provide cross-functional transparency of the clinical trial(s) progress to ensure team is efficiently progressing forward with deliverables, including deliverables from CRO and other partners. - Organize internal and external meetings (development of agendas, minutes, and presentations). - Manage ancillary supplies for clinical trials. - Support risk management including risk assessment, mitigation planning, and internal and external audit preparation and follow-up. - Contribute to development of clinical study plans and manuals, including version tracking and team training. - Provide ### Senior Director, Regulatory Affairs - Bicara Therapeutics Inc - Location: Boston, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://jobs.ashbyhq.com/bicara-therapeutics/96bde11e-c940-4688-9d85-25bcd24dcabb - Excerpt: Senior Director, Regulatory Affairs Boston, MA, United States Position Overview Bicara Therapeutics is seeking a strategic and experienced Senior Director of Regulatory Affairs to lead and execute US regulatory strategy for our biologics pipeline. Reporting to the VP, Regulatory Affairs, you will serve as the primary US regulatory lead with a core focus on BLA strategy and execution-from IND through BLA submission and approval. You will manage a small team of Regulatory Affairs professionals, providing mentorship and oversight while working in close partnership with the VP to ensure alignment on regulatory direction, agency interactions, and submission timelines. This role is based in our Boston office and follows a hybrid schedule, with three in-office days each week. Responsibilities - Develop and execute integrated global regulatory strategies to advance investigational oncology assets from early development through approval and lifecycle management, partnering closely with the VP, Regulatory Affairs. - Serve as the global regulatory lead on assigned programs, providing strategic guidance to cross-functional teams (Clinical, Nonclinical, CMC, Biostatistics, Clinical Operations, Medical Affairs, and Commercial). - Lead the planning, preparation, and submission of high-quality regulatory documents to FDA, including INDs, briefing documents, orphan/breakthrough designations, amendments, annual reports, and NDA/BLAs. Collaborate with external vendors for submissions in other regions. - Plan, prepare, and lead health authority interactions, including pre-IND, Type B/C, EOP, and pre-submission meetings; coach and prepare cross-functional teams for successful engagements. - Lead and manage a small US team of regulatory professionals; set priorities, allocate work, and cultivate a collaborative, accountable team culture. ### Therapeutic Area Manager (TAM), Hematology - Pennsylvania Ecosystem - Genentech, Inc. - Location: Philadelphia, Pennsylvania, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/Philadelphia/Therapeutic-Area-Manager--TAM---Hematology---Pennsylvania-Ecosystem_202606-114050-1/apply - Excerpt: Therapeutic Area Manager (TAM), Hematology - Pennsylvania Ecosystem Philadelphia, Pennsylvania, United States of America Embrace the opportunity to become a Therapeutic Area Manager, Hematology, and drive impactful patient outcomes in the Philadelphia ecosystem. Leverage your expertise in oncology and healthcare systems to lead cross-functional teams, optimize product access, and shape clinical strategies. Make a difference in rare disease care with Genentech. ### Therapeutic Area Manager (TAM), Breast - Pennsylvania Ecosystem - Genentech, Inc. - Location: Wilmington, Delaware, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/Delaware/Therapeutic-Area-Manager--TAM---Breast---Pennsylvania-Ecosystem_202606-114052/apply - Excerpt: Therapeutic Area Manager (TAM), Breast - Pennsylvania Ecosystem Wilmington, Delaware, United States of America Embrace the opportunity to become a Therapeutic Area Manager, Breast, and drive impactful patient outcomes in the Pennsylvania ecosystem. Leverage your expertise in healthcare sales, account management, and cross-functional collaboration to optimize product access and support innovative treatments. Make a difference in the rare disease community with Genentech. ### Therapeutic Area Head – Respiratory - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $395K-$425K - Posted: 2026-06-11 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5160938007 - Excerpt: Therapeutic Area Head – Respiratory Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Therapeutic Area (TA) Head, Respiratory - Clinical Development. In this ### Therapeutic Area Lead Vaccines & Infectious Diseases - Merck & Co., Inc. - Location: POL - Mazowieckie Wojewodztwo - Warsaw (Trade Center) (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/POL---Mazowieckie-Wojewodztwo---Warsaw-Trade-Center/Therapeutic-Area-Lead-Vaccines---Infectious-Diseases_R397207-1 - Excerpt: Therapeutic Area Lead Vaccines & Infectious Diseases POL - Mazowieckie Wojewodztwo - Warsaw (Trade Center) posted: Posted 2 Days Ago ### Clinical Trial Manager - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-05-11 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/3913773 - Excerpt: Clinical Trial Manager Viking Therapeutics, Inc. Clinical Trial Manager ### Drug Safety Manager - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-03-19 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4014908 - Excerpt: Drug Safety Manager Viking Therapeutics, Inc. Drug Safety Manager ### Senior/Executive Director, Health Economics & Outcomes Research (HEOR) - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-29 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4127771 - Excerpt: Senior/Executive Director, Health Economics & Outcomes Research (HEOR) Viking Therapeutics, Inc. Senior/Executive Director, Health Economics & Outcomes Research (HEOR) ### Associate Director, Formulation Development - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4079847 - Excerpt: Associate Director, Formulation Development Viking Therapeutics, Inc. Associate Director, Formulation Development ### Finance Enterprise Partner - Therapeutic Area - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-05-08 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Finance-Enterprise-Partner---Therapeutic-Area_202603-108237-1/apply - Excerpt: Finance Enterprise Partner - Therapeutic Area South San Francisco, California, United States of America Embrace the role of a Finance Enterprise Partner - Therapeutic Area and drive strategic financial decisions in a dynamic pharmaceutical environment. Collaborate with cross-functional leaders, lead financial planning, and optimize portfolio performance. Shape the future of healthcare finance while supporting commercial, medical, and market access initiatives. Grow your career with us! ### Principal Scientist, Peptide Therapeutics - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-02-24 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Principal-Scientist--Peptide-Therapeutics_202602-103654/apply - Excerpt: Principal Scientist, Peptide Therapeutics South San Francisco, California, United States of America This is a primarily lab-based, technical leadership position within the Peptide Therapeutics department. In this lab-based leadership role, you will combine hands-on synthetic expertise with strategic... ### Therapeutic Area Policy Director - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-01 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Therapeutic-Area-Policy-Director_202605-112975-1/apply - Excerpt: Therapeutic Area Policy Director South San Francisco, California, United States of America Exciting opportunity for a strategic policy director to shape healthcare policy and optimize patient access across diverse therapeutic areas. Lead cross-functional teams, influence policy at the highest levels, and drive strategic readiness for innovative therapies. Join us to make a significant impact on patient outcomes and healthcare innovation. ### Director of Process Validation - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-09 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4075036 - Excerpt: Director of Process Validation Viking Therapeutics, Inc. Director of Process Validation ### Medical Science Liaison Director/Lead - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-27 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4116882 - Excerpt: Medical Science Liaison Director/Lead Viking Therapeutics, Inc. Medical Science Liaison Director/Lead ### Executive Director, Therapeutic Area Lead, CVRM - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2025-12-17 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Executive-Director--Therapeutic-Area-Lead--CVRM_202512-132040-1/apply - Excerpt: Executive Director, Therapeutic Area Lead, CVRM South San Francisco, California, United States of America Exciting opportunity for an Executive Director, Therapeutic Area Lead and drive medical strategy, innovation, and leadership in a dynamic healthcare environment. Lead high-impact teams, shape clinical trials, and collaborate across functions to advance patient outcomes. If you have deep medical expertise and proven people management skills, this is your next career-defining opportunity. ### Associate Therapeutic Development Manager - Merck & Co., Inc. - Location: HKG - Hong Kong Island - Hong Kong (Lee Garden Two) (unspecified) - Salary: Not disclosed - Posted: 2026-05-27 - Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/HKG---Hong-Kong-Island---Hong-Kong-Lee-Garden-Two/Associate-Therapeutic-Development-Manager_R400021 - Excerpt: Associate Therapeutic Development Manager HKG - Hong Kong Island - Hong Kong (Lee Garden Two) posted: Posted 16 Days Ago ### Therapeutic Area Analytics & Insights Director - Respiratory - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Therapeutic-Area-Analytics---Insights-Director---Respiratory_202605-113485-1/apply - Excerpt: Therapeutic Area Analytics & Insights Director - Respiratory South San Francisco, California, United States of America Join our team as Director, Therapeutic Area Analytics & Insights - Respiratory and drive high-impact, data-driven strategies for a leading healthcare portfolio. Leverage your expertise in analytics, stakeholder management, and respiratory expertise to shape business outcomes, collaborate with cross-functional teams, and deliver actionable insights that improve patient care and outcomes. ### Executive Director, Therapeutic Strategy Leader, APAC - Fortrea Holdings Inc - Location: Shanghai, China (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Shanghai/ED--Therapeutic-Strategy-Leader--APAC_261967/apply - Excerpt: Executive Director, Therapeutic Strategy Leader, APAC Shanghai, China This role is for upcoming future opportunities that may arise at Fortrea. Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll i... ### Principal Product Leader, Therapeutics Discovery - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Principal-Product-Leader--Therapeutics-Discovery_202606-114878-1/apply - Excerpt: Principal Product Leader, Therapeutics Discovery South San Francisco, California, United States of America Exciting opportunity for a Principal Product Leader in Therapeutics Discovery, driving strategy and innovation for cutting-edge products in drug discovery. Collaborate with top scientists, shape product vision, and accelerate impactful solutions in a dynamic, data-driven environment. Make a difference in advancing life-changing therapies and scientific discovery at the forefront of biotechnology. ### Senior Principal Scientist, Peptide Therapeutics - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-01-08 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Senior-Principal-Scientist--Peptide-Therapeutics_202510-126773/apply - Excerpt: Senior Principal Scientist, Peptide Therapeutics South San Francisco, California, United States of America You will lead the Medicinal Chemistry efforts for a highly integrated and collaborative team, applying your deep scientific expertise to solve complex drug discovery challenges and drive projects forw... ### Vice President, Commercial Manufacturing Operations - VERA Therapeutics INC - Location: Remote (remote) - Salary: $248K-$375K - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4273981009 - Excerpt: Vice President, Commercial Manufacturing Operations Remote Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics' mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics' lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell-mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit www.veratx.com . Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do-from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases. Position Summary: The Vice President, Manufacturing Operations will report ### Information Security Lead - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $130K-$200K - Posted: 2026-02-25 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8414783002 - Excerpt: Information Security Lead New York, NY Who We Are: Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As Information Security Lead, you'll be at the forefront of safeguarding our groundbreaking digital therapeutics. We're seeking an individual with deep technical expertise in information security in the healthcare sector, ready to tackle complex challenges and pioneer innovative solutions. This isn't just a role; it's an opportunity to build, mentor, and inspire a high-performing team, while strategically collaborating across ### Senior Director/Vice President, Market Access - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $180K-$280K - Posted: 2026-04-21 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8515744002 - Excerpt: Senior Director/Vice President, Market Access New York, NY Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As a Senior Director / Vice President of Market Access, you will be the backbone of the commercial organization. You will design the financial architecture of the product, shape the external policy and regulatory environments to support PDTs, and ensure long term viability of the PDT category. The role reports to the Chief Commercial Officer and ### Associate Director, Device Development - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $180K-$200K - Posted: 2026-05-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5145512007 - Excerpt: Associate Director, Device Development Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary Apogee Therapeutics is seeking an Associate Director, Device Development to join the Technical Operations team ### Associate Director, Clinical Development (Clinical Science) – Immunology - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $180K-$210K - Posted: 2026-05-28 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5146485007 - Excerpt: Associate Director, Clinical Development (Clinical Science) – Immunology Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary Apogee Therapeutics is seeking an experienced Clinical Scientist for an Associate ### DTx Quality Engineer (6 Month Contract) - Click Therapeutics - Location: Remote (remote) - Salary: $100-$120/hr - Posted: 2026-05-04 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8534499002 - Excerpt: DTx Quality Engineer (6 Month Contract) Remote Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. Responsibilities: - Initiate and manage complaint records for investigational and commercial SaMD applications from receipt to closure in a timely and compliant manner. - Maintain all records in a state of audit readiness ensuring compliance with internal procedures and applicable regulatory requirements. - Evaluate incoming complaint information on whether reporting to applicable government agencies is required. - Coordinate with cross-functional ### Join Our Talent Community - Click Therapeutics - Location: New York, NY or Boston, MA (unspecified) - Salary: Not disclosed - Posted: 2024-12-16 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/7776029002 - Excerpt: Join Our Talent Community New York, NY or Boston, MA Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About Our Talent Community: Don't see a perfect fit for your skills right now? We're constantly growing and adding new positions. Join our talent community to stay informed about upcoming opportunities that align with your unique background and experience. Be the first to know about exciting new roles! While joining our talent community doesn't constitute a formal ### Senior Director/VP, Medical Affairs - Click Therapeutics - Location: New York, NY, Boston, MA or Remote (remote) - Salary: $180K-$280K - Posted: 2026-04-29 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8525471002 - Excerpt: Senior Director/VP, Medical Affairs New York, NY, Boston, MA or Remote Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As the Senior Director / Vice President of Medical Affairs, you will be the scientific heartbeat of the organization. You will act as the scientific authority for CT-155. This team generates the evidence (RWE/OLE) needed to prove clinical value and economic impact, supplying the "raw material" that Marketing and Access teams leverage. The ### Sr. Analyst/Manager, Access, Policy and Commercial Operations - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $125K-$180K - Posted: 2026-04-29 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8526277002 - Excerpt: Sr. Analyst/Manager, Access, Policy and Commercial Operations New York, NY Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: The Senior Associate provides foundational execution and analytical support across access, policy, and commercial operations. This role is ideal for candidates early in their careers who are eager to build expertise, take on increasing responsibility, and use AI-driven tools to work smarter and faster. This position is based out of Click's headquarters located in ### Senior Director/Vice President, Patient, HCP, and Payer Marketing - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $180K-$280K - Posted: 2026-04-21 - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8515720002 - Excerpt: Senior Director/Vice President, Patient, HCP, and Payer Marketing New York, NY Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As a Senior Director / Vice President of HCP and Payer Marketing, you will shape the overall marketing strategy for near-term launch products and build a best in class marketing organization to execute that vision. You and your team will define the brand strategy and create the narrative and materials that drive behavior ### Senior Scientist, Cellular Pharmacology - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Senior-Scientist--Cellular-Pharmacology_202606-114286/apply - Excerpt: Senior Scientist, Cellular Pharmacology South San Francisco, California, United States of America Join our team as a Senior Scientist in Cellular Pharmacology and drive innovation in drug discovery for diverse therapeutic areas. Lead advanced pharmacology assays, collaborate with multidisciplinary teams, and shape the future of cell-based therapies. If you have expertise in iPSCs, CRISPR gene editing, and ophthalmology/neuroscience therapeutics, we want to hear from you! ### Associate Director, Clinical Supply Chain Management - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $170K-$190K - Posted: 2026-04-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5097898007 - Excerpt: Associate Director, Clinical Supply Chain Management Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a highly motivated and results-oriented individual to join Apogee Therapeutics ### Therapeutic Specialist, Vision Care, Southwestern Ontario and Niagara - AbbVie Inc. - Location: Remote | London, ON, Canada (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013455576-therapeutic-specialist-vision-care-southwestern-ontario-and-niagara - Excerpt: Therapeutic Specialist, Vision Care, Southwestern Ontario and Niagara Remote | London, ON, Canada Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. When choosing your career path, choose to be remarkable. Job Description: We are presently recruiting for the role of Therapeutic Specialist - Vision Care for Southwestern Ontario and Niagara , reporting to Lisa Culley, District Sales Manager in Ontario for Vision Care. The candidate will be responsible for managing and leading business development in some of our largest customer key accounts in Southwestern Ontario and Niagara. The product portfolio includes dry eye prescription and OTC products. The Therapeutic Specialist - Vision Care for Southwestern Ontario and Niagara is intended to be the face of AbbVie to identified Key Accounts to continue to build on and develop the long-term customer relationships across the vision care portfolio. Position Overview and Role Description: The successful candidate will be responsible for cultivating relationships with existing customers and expanding awareness and use of focused AbbVie Vision Care products in the Dry Eye portfolio. The Therapeutic Specialist - Vision Care for Southwestern Ontario ### Medical Advisor, Gastro - AbbVie Inc. - Location: Seoul, Seoul, Korea, republic of (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013290166-medical-advisor-gastro - Excerpt: Medical Advisor, Gastro Seoul, Seoul, Korea, republic of Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: PRIMARY FUNCTION/OBJECTIVE To lead medical team and activities in responsible therapeutic areas. Set and execute Medical Affairs strategies for the responsible therapeutic areas. To set and deliver medical affairs strategies which generate, evaluate and communicate scientific evidence to support the needs of health care professionals and patients in covered therapeutic areas, in line with the strategic priorities of the brand and company, and all prevailing governance requirements. To make recommendations regarding staffing levels and structure for the team, and to plan and manage budget within prevailing finance guidance. To support the Korea Medical Director to build the organisation, ensuring the medical department is fully integrated to support the strategy and affiliate business, while being functionally independent and operating within a culture of ethical and compliant behaviour. Main responsibilities: Fulfill the responsibilities of a Medical Advisor in the Gastroenterology therapeutic area. Develop and execute the annual medical affairs strategy and plans, and contribute to long-range strategic plans for the assigned therapeutic ### Director, Head of Product Management – AI-Enabled Precision Medicine (Therapeutics & Innovations) - Natera, Inc. - Location: US Remote (remote) - Salary: $185K-$231K - Posted: 2026-05-15 - Apply: https://job-boards.greenhouse.io/natera/jobs/5994721004 - Excerpt: Director, Head of Product Management – AI-Enabled Precision Medicine (Therapeutics & Innovations) US Remote Director, Head of Product Management - AI-Enabled Precision Medicine (Therapeutics & Innovations) About Us We are redefining the future of precision medicine by integrating AI with healthcare to create next-generation, precision treatment modalities. Our multidisciplinary team is building products at the intersection of clinical data, multi-omics, and machine learning-unlocking entirely new approaches to drug development and patient care. Within the Therapeutics & Innovations Business Unit, we are developing a new category that bridges diagnostics and therapeutics. Our platform combines deep scientific expertise with proprietary datasets to power AI-enabled solutions that can transform how therapies are discovered, developed, and deployed. We are looking for a product leader who can translate this potential into real, scalable products-owning the strategy, roadmap, and execution to bring these innovations to market. The Role We are seeking a Director / Head of Product Management to lead product strategy and execution for our AI-enabled therapeutics platform. This is a highly cross-functional leadership role at the center of science, engineering, clinical development, and commercial strategy. You will define what we build, why it matters, and how it creates value-for biopharma partners, clinicians, and ultimately patients. You will own the product lifecycle end-to-end: from concept and validation through development, launch, and iteration. This role requires a rare blend of scientific fluency, product rigor, and commercial instinct . You will work closely with R&D, AI, medical, business development, and marketing to ensure our products are scientifically ### Manager, MHI Business Analytics - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013473367-manager-mhi-business-analytics - Excerpt: Manager, MHI Business Analytics North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The ME (Medical Engagement) team within MHI (Medical Affairs + Health Impact) plays an instrumental role in supporting Therapeutic Area (TA) strategy and informing tactical execution for AbbVie's therapeutic areas globally. As Manager, Business Analytics on the Medical Engagement team you will execute standard and ad-hoc analytic delivery. Analytic output will be used to inform strategic opportunities, provide recommendations, elevate organizational data maturation, and develop sustainable, automated analytic processes. This role requires strong data analytic capabilities across various data ecosystems. Responsibilities: Perform and lead analytics projects across the various AbbVie therapeutic areas and the MHI organization through claims and business data analysis by leveraging both internal and external datasets including big data sources to shape utilization of strategic insight opportunities. Demonstrate strong understanding of the U.S. healthcare landscape and key AbbVie Therapeutic areas to identify and proactively address opportunities and threats. Build collaborative relationships with internal stakeholders (e.g., HEOR, RWD/E teams, therapeutic area teams, operations, and BTS/IR to ### Associate Director, Statistical Programming - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $190K-$210K - Posted: 2026-04-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5097750007 - Excerpt: Associate Director, Statistical Programming Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an Associate Director of Statistical Programming. In this position you will be ### Senior Manager, Clinical Biomarker Operations - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $150K-$170K - Posted: 2026-04-22 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5117623007 - Excerpt: Senior Manager, Clinical Biomarker Operations Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary The Department of Research and Translational Medicine is seeking a Clinical Biomarker Operations Sr. ### Director, Clinical Development (Clinical Science) - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $230K-$260K - Posted: 2026-05-15 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5138987007 - Excerpt: Director, Clinical Development (Clinical Science) Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an experienced non-MD Clinical Scientist. As a Director in Clinical Development, ### Director, Data Management and Systems - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $215K-$245K - Posted: 2026-06-10 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5161364007 - Excerpt: Director, Data Management and Systems Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary The Director of Data Management and Systems (DM) is a strategic and operational leader ### Clinical Trial Manager - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $145K-$160K - Posted: 2026-04-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5098120007 - Excerpt: Clinical Trial Manager Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Clinical Trial Manger (CTM) to join our growing Clinical Operations team! In ### Director, AI Enablement - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $225K-$250K - Posted: 2026-05-19 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5141496007 - Excerpt: Director, AI Enablement Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Director, IT - AI Enablement . In this newly created role, you ### Associate Director, Biostatistics - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $195K-$225K - Posted: 2026-01-05 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5015149007 - Excerpt: Associate Director, Biostatistics Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an Associate Director of Biostatistics. In this position you will be acting as ### Senior Specialist, Supply Chain Management - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $115K-$130K - Posted: 2026-06-08 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5158901007 - Excerpt: Senior Specialist, Supply Chain Management Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary - Review clinical trial synopsis and/or protocols to understand IMP supply and demand requirements. ### Senior Associate, Regulatory Affairs - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $120K-$135K - Posted: 2026-05-06 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5130456007 - Excerpt: Senior Associate, Regulatory Affairs Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Senior Associate, Regulatory Affairs. This newly created role offers an opportunity ### Associate Director, Inflammation Biology - Apogee Therapeutics Inc - Location: Hybrid (hybrid) - Salary: $185K-$205K - Posted: 2026-06-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5152861007 - Excerpt: Associate Director, Inflammation Biology Hybrid About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary The Department of Research and Translational Medicine is seeking an Associate Director , Biology . ### Senior Manager, Regulatory Affairs Project Management - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $150K-$170K - Posted: 2026-03-19 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5083978007 - Excerpt: Senior Manager, Regulatory Affairs Project Management Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an experienced biotech project manager to optimize planning, execution, and ### Senior Manager, Medical Writing - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $160K-$180K - Posted: 2026-05-08 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5132727007 - Excerpt: Senior Manager, Medical Writing Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an experienced and motivated medical writer who is responsible for providing clinical ### Associate Director, Monitoring Oversight Management - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $180K-$205K - Posted: 2025-12-15 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5005031007 - Excerpt: Associate Director, Monitoring Oversight Management Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an Associator Director, Monitoring Oversight Management, to manage Apogee's Oversight CRAs ### Associate Director, Biomarker Development - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $190K-$210K - Posted: 2026-05-29 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5148737007 - Excerpt: Associate Director, Biomarker Development Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary The Department of Research and Translational Medicine is seeking an Associate Director, Biomarker Development. This ### Sr. Medical Director, Gastroenterology - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $350K-$375K - Posted: 2026-05-18 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5104690007 - Excerpt: Sr. Medical Director, Gastroenterology Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Sr. Medical Director to lead the EoE (eosinophilic esophagitis) clinical development ### Associate Director, Manufacturing Science and Technology - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $175K-$195K - Posted: 2026-01-09 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5020220007 - Excerpt: Associate Director, Manufacturing Science and Technology Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a dynamic and experienced MSAT Associate Director to support late-stage ### Manager, Clinical Business Operations - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $145K-$160K - Posted: 2026-03-13 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5078580007 - Excerpt: Manager, Clinical Business Operations Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Manager, Clinical Business Operations to join the Clinical Operations team at ### Senior Director, Channel Strategy and Patient Support - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $280K-$305K - Posted: 2026-05-13 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5137040007 - Excerpt: Senior Director, Channel Strategy and Patient Support Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary Channel Strategy - Conduct market research on distribution strategies and trends within ### Associate Director, GMP Quality Assurance - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $165K-$195K - Posted: 2026-04-27 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5108935007 - Excerpt: Associate Director, GMP Quality Assurance Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a dynamic and results-driven Associate Director of GMP Quality Assurance (QA) ### Medical Science Liaison - Respiratory - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $210K-$235K - Posted: 2026-05-15 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5138739007 - Excerpt: Medical Science Liaison - Respiratory Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an experienced Medical Science Liaison (MSL) with expertise in asthma and ### Associate Director, Scientific Communications - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $170K-$195K - Posted: 2026-06-10 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5161356007 - Excerpt: Associate Director, Scientific Communications Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a motivated and experienced Associate Director, Scientific Communications to serve as a ### Clinical Monitoring Manager - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $150K-$170K - Posted: 2026-03-02 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5052304007 - Excerpt: Clinical Monitoring Manager Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Clinical Monitoring Manager to oversee in-house Oversight CRAs that will oversee CRO ### Medical Science Liaison Dermatology - Northeast - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $210K-$250K - Posted: 2026-05-29 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5149758007 - Excerpt: Medical Science Liaison Dermatology - Northeast Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Key Responsibilities - Clinical Support - Collaborate with the clinical study teams to provide medical ### Senior Director, Statistical Programming - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $270K-$295K - Posted: 2026-04-30 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5125373007 - Excerpt: Senior Director, Statistical Programming Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary - Support the statistical programming function by implementing programming processes, standards, and SOPs for clinical ### Director, Drug Product Development - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $210K-$235K - Posted: 2026-01-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5021986007 - Excerpt: Director, Drug Product Development Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Director, Drug Product Development to develop protein drug product presentations and ### Medical Director - Dermatology - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $290K-$330K - Posted: 2026-06-01 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5138734007 - Excerpt: Medical Director - Dermatology Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Medical Director to oversee clinical execution and medical monitoring of dermatology ### Executive Director, GMP Quality Assurance - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $275K-$305K - Posted: 2026-04-17 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5112880007 - Excerpt: Executive Director, GMP Quality Assurance Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an Executive Director of GMP Quality Assurance (QA) to serve as ### Medical Director Pharmacovigilance - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $285K-$330K - Posted: 2026-06-01 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5151650007 - Excerpt: Medical Director Pharmacovigilance Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Medical Director, Pharmacovigilance to join the Apogee Clinical Development team. In this ### Director, Insights and Market Development - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $235K-$255K - Posted: 2026-05-14 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5137582007 - Excerpt: Director, Insights and Market Development Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking an experienced Director, Insights and Market Development to serve as a ### Senior Manager, Regulatory Affairs - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $155K-$175K - Posted: 2026-04-24 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5120442007 - Excerpt: Senior Manager, Regulatory Affairs Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Senior Manager, Regulatory Affairs. This newly created role offers an opportunity ### MSL/Senior MSL, Dermatology - Miami, Florida - AbbVie Inc. - Location: Remote | Miami, FL, United States (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012980357-msl-senior-msl-dermatology-miami-florida - Excerpt: MSL/Senior MSL, Dermatology - Miami, Florida Remote | Miami, FL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The MSL/Senior MSL is a field based scientific expert that strategically supports the research and business objectives of a designated therapeutic area across the product life cycle for a specific geography/territory The MSL/Senior MSL is the primary communicator of AbbVie science within a specific geography with healthcare professionals. The MSL/Senior MSL develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to AbbVie initiatives in assigned therapeutic areas. The MSL/Senior MSL is viewed as a peer scientific expert in a designated therapeutic area/product. Combined with strong strategic vision, market therapeutic area awareness, as well as clinical expertise, the MSL/Senior MSL serve as a conduit of information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by AbbVie. The MSL/Senior MSL works closely with other AbbVie personnel to ensure information, education, and research needs of ### MSL/Senior MSL - Dermatology, Jersey City, NJ - AbbVie Inc. - Location: Remote | Trenton, NJ, United States (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013502196-msl-senior-msl-dermatology-jersey-city-nj - Excerpt: MSL/Senior MSL - Dermatology, Jersey City, NJ Remote | Trenton, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The MSL/Senior MSL is a field based scientific expert that strategically supports the research and business objectives of a designated therapeutic area across the product life cycle for a specific geography/territory The MSL/Senior MSL is the primary communicator of AbbVie science within a specific geography with healthcare professionals. The MSL/Senior MSL develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to AbbVie initiatives in assigned therapeutic areas. The MSL/Senior MSL is viewed as a peer scientific expert in a designated therapeutic area/product. Combined with strong strategic vision, market therapeutic area awareness, as well as clinical expertise, the MSL/Senior MSL serve as a conduit of information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized by AbbVie. The MSL/Senior MSL works closely with other AbbVie personnel to ensure information, education, and research needs of healthcare professionals are met ### Director, Regulatory Affairs - Nurix Therapeutics Inc - Location: Brisbane, California, United States (unspecified) - Salary: Not disclosed - Posted: 2026-05-04 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/nurix/jobs/8535319002 - Excerpt: Director, Regulatory Affairs Brisbane, California, United States Position Title: Director, Regulatory Affairs (Strategy, Immunology and Inflammation) Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease. Nurix Therapeutics, Inc. is seeking a Director, Regulatory Affairs (Strategy, I&I) to join the Regulatory team. The successful candidate will be a core member of the Regulatory team and will serve as the global regulatory lead (GRL) for the immunology and inflation therapeutic area. This role will be responsible for developing the global regulatory strategy in collaboration with key internal stakeholders, as well as tactical implementation of that strategy guiding and executing compliant, high quality, nonclinical and clinical submissions and interactions in support of early development, registration and life cycle management activities. This position works cross-functionally with regulatory affairs and clinical development organizations to facilitate the completion of regulatory filing documentation according to company timelines. It also ensures adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as required. This position is ### Executive Director, Medical Affairs - Eosinophilic Esophagitis (EoE) - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $305K-$340K - Posted: 2026-05-18 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_I_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5139934007 - Excerpt: Executive Director, Medical Affairs - Eosinophilic Esophagitis (EoE) Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a strategic, highly experienced Executive Director, Medical Affairs ### Therapeutic Mentor - Centerstone - Location: Bradenton, Florida (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://centerstone.wd5.myworkdayjobs.com/CenterstoneCareers/job/Bradenton-Florida/Therapeutic-Mentor_JR-030233 - Excerpt: Therapeutic Mentor Bradenton, Florida posted: Posted 2 Days Ago ### Senior Scientist I, siRNA in vitro Biology - AbbVie Inc. - Location: Cambridge, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012913220-senior-scientist-i-sirna-in-vitro-biology - Excerpt: Senior Scientist I, siRNA in vitro Biology Cambridge, MA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are dedicated to solving some of the world's most complex and serious diseases. Within AbbVie's Biotherapeutics and Genetic Medicine (BGM) organization, our siRNA team is advancing therapeutic programs from early discovery through development, applying rigorous biology and data-driven decision making to build differentiated RNA medicines. AbbVie is seeking a Senior Scientist I with deep, hands-on expertise in siRNA therapeutic discovery to join the siRNA group within Biotherapeutics and Genetic Medicine (BGM). This role will involve designing and executing innovative experimental approaches to address key scientific challenges related to oligonucleotide therapeutics. The successful candidate will drive scientific innovation, identify new methods and techniques, and collaborate across functions to support the development of novel RNA-based therapies. This role is best suited for candidates with direct, hands-on experience in therapeutic siRNA discovery, where siRNA biology directly informed experimental and program-level decisions. Responsibilities Independently lead in vitro siRNA discovery biology, including experimental strategy, ### Director, Finance Oncology and OED - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013517666-director-finance-oncology-and-oed - Excerpt: Director, Finance Oncology and OED North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The primary objective of this position is to provide financial leadership, study forecasting, and business support for Oncology and OED therapeutic areas dynamic clinical portfolio within R&D Therapeutics, with portion of ~$2.5Bn spend. Specifically, this role partners closely with the therapeutic leadership teams to establish prioritization and align related programs across the respective therapeutic area and business partners to optimize available funding and ensure financial commitments are met, interacting with all levels of finance and business leadership. Core Responsibilities: Financial Planning and Analysis : Proactively lead the planning processes [Plan, LBE and LRP] ensuring accurate and timely integration of clinical study forecasts and other Externals spend types (PMed, CMC, etc.), ensuring senior management input to meet overall R&D / Corporate deadlines and deliverables. Ensure financial planning and reporting deliverables are accurate, clear and concise for Executive level review and approval. Ensure alignment of clinical assumptions with Commercial finance for Plan and LRP cycles. Sponsor and drive initiatives ### Area TA Lead (Director) Neuroscience, Intercontinental Medical Affairs - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013297996-area-ta-lead-director-neuroscience-intercontinental-medical-affairs - Excerpt: Area TA Lead (Director) Neuroscience, Intercontinental Medical Affairs Mettawa, IL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The Area TA Lead will act as the Intercontinental Neuroscience Lead, providing medical/scientific strategic and operational input into core medical affairs activities and relevant scientific and technical training to Affiliate Therapeutic Area resources. Will work closely with Area commercial teams to provide strategic medical input into core Neuroscience assets strategies, and to support medical/marketing activities and market access; provide scientific and technical support for assigned products. Develops and maintains professional and credible relationships with key external experts and professional societies; provides therapeutic expertise in interactions with regulators and other external groups; develops innovative research concepts for clinical data generation and communication. Collaborates with clinical development, global, International teams, and affiliates to support pipeline execution and acceleration efforts across Intercontinental geographies for neuroscience assets. *Hybrid (3x per week on-site) in Mettawa, IL. Key Responsibilities Include : Develops Area therapeutic Evidence Generation plan and Area therapeutic strategic initiatives Brings insights and knowledge from ### Analyst, Finance - US Therapeutics - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012993586-analyst-finance-us-therapeutics - Excerpt: Analyst, Finance - US Therapeutics Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The purpose of the Finance Analyst role is to support operational activities within the US Therapeutics Divisional Headquarters team, focusing on Long Range Plan (LRP) and Plan Cycle processes. As a Financial Analyst, you will play a pivotal role in executing and advancing key processes, delivering insightful analysis, and enabling team priorities, while contributing meaningfully to the company's long-term success and helping shape a best-in-class financial planning and analysis function. Responsibilities This role reports to the US Commercial FP&A Senior Manager and supports the Plan and Long-Range Plan review cycles. As a member of the US Therapeutics finance team, you will provide accurate and timely analysis to meet important due dates and project timelines. Assist with cycle planning activities, including developing guidance, creating mock books, preparing templates and schedules. Perform financial analyses of the P&L throughout the review cycles to ensure the accuracy and completeness of data submitted by business partners. Effective interaction with cross functional and business unit ### MSL/Sr MSL, Migraine (IA, MN, NE, and Central MO) - AbbVie Inc. - Location: Remote | Des Moines, IA, United States (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012913499-msl-sr-msl-migraine-ia-mn-ne-and-central-mo- - Excerpt: MSL/Sr MSL, Migraine (IA, MN, NE, and Central MO) Remote | Des Moines, IA, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Medical Science Liaison is a field based scientific expert who strategically supports the scientific and business objectives of a designated therapeutic area across the product life cycle for a specific geography/territory. The Medical Science Liaison is the primary communicators of AbbVie science within a specific geography with healthcare professionals. The Medical Science Liaison combines strong strategic vision clinical expertise, therapeutic area awareness, serving as a conduit of information to a cross functional customer base internally within AbbVie. The Medical Science Liaison develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to AbbVie initiatives in assigned therapeutic areas. The Medical Science Liaison facilitates the exchange of scientific information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies. Responsibilities Focus on mastery of scientific content, materials, disease state and therapeutic area to establish themselves as a scientific expert. Identify, ### Director, Finance Immunology - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013521686-director-finance-immunology - Excerpt: Director, Finance Immunology North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The primary objective of this position is to provide financial leadership, study forecasting, and business support for Immunology therapeutic areas dynamic clinical portfolio within R&D Therapeutics, with portion of ~$2.5Bn spend. Specifically, this role partners closely with the therapeutic leadership teams to establish prioritization and align related programs across the respective therapeutic area and business partners to optimize available funding and ensure financial commitments are met, interacting with all levels of finance and business leadership. Core Responsibilities: Financial Planning and Analysis : Proactively lead the planning processes [Plan, LBE and LRP] ensuring accurate and timely integration of clinical study forecasts and other Externals spend types (PMed, CMC, etc.), ensuring senior management input to meet overall R&D / Corporate deadlines and deliverables. Ensure financial planning and reporting deliverables are accurate, clear and concise for Executive level review and approval. Ensure alignment of clinical assumptions with Commercial finance for Plan and LRP cycles. Sponsor and drive initiatives to significantly improve agility ### Therapeutic Medical Scientist, Italy - Cytokinetics INC - Location: Milan, Italy (unspecified) - Salary: Not disclosed - Posted: 2026-04-14 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/cytokinetics/jobs/8464805002 - Excerpt: Therapeutic Medical Scientist, Italy Milan, Italy Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Therapeutic Medical Scientist (Medical Science Liaison) Reporting to the Senior Medical Director for Italy, the TMS is a scientific professional who serves as a key field-based scientific resource for healthcare providers, patients, industry partners and internal colleagues. This role will come with high visibility in our company including critical cross-functional relationships across Medical Affairs, Clinical Development / Operations, and Commercial. This role will focus on key opinion leaders and other HCP's in the hypertrophic cardiomyopathy therapeutic area, but also support pipeline products in development. Our passion is anchored in rigorous and diligent scientific and clinical approaches to the discovery and development of novel mechanism therapeutics. With gratitude for the commitments and convictions of our employees who are inspired by the courage of patients we aim to serve, we believe Cytokinetics will continue to be a pioneering, values-driven, sustainable, fully integrated biopharmaceutical company. Role and Responsibilities: Identify national, regional, and local Key Opinion Leaders (KOLs) involved in the provision of cardiovascular care within institutional care centres and engage them in proactive and reactive scientific exchange Maintain and enhance existing scientific collaboration and ### Director, Finance Specialty/Toxin - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013517364-director-finance-specialty-toxin - Excerpt: Director, Finance Specialty/Toxin North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The primary objective of this position is to provide financial leadership, study forecasting, and business support for Specialty/Toxin therapeutic areas dynamic clinical portfolio within R&D Therapeutics, with portion of ~$2.5Bn spend. Specifically, this role partners closely with the therapeutic leadership teams to establish prioritization and align related programs across the respective therapeutic area and business partners to optimize available funding and ensure financial commitments are met, interacting with all levels of finance and business leadership. Core Responsibilities: Financial Planning and Analysis : Proactively lead the planning processes [Plan, LBE and LRP] ensuring accurate and timely integration of clinical study forecasts and other Externals spend types (PMed, CMC, etc.), ensuring senior management input to meet overall R&D / Corporate deadlines and deliverables. Ensure financial planning and reporting deliverables are accurate, clear and concise for Executive level review and approval. Ensure alignment of clinical assumptions with Commercial finance for Plan and LRP cycles. Sponsor and drive initiatives to significantly improve agility ### Therapeutic Specialist - Gilead Sciences - Location: Spain - Alicante (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Spain---Alicante/Therapeutic-Specialist_R0052600 - Excerpt: Therapeutic Specialist Spain - Alicante posted: Posted 2 Days Ago ### Therapeutic Specialist I - Gilead Sciences - Location: China - Kunming (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Kunming/Therapeutic-Specialist-I_R0052372-2 - Excerpt: Therapeutic Specialist I China - Kunming posted: Posted 30+ Days Ago ### Submit your resume for future full time openings - Beam Therapeutics Inc - Location: Cambridge, MA and Durham, NC (unspecified) - Salary: Not disclosed - Posted: 2022-08-03 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://job-boards.greenhouse.io/beamtherapeutics/jobs/6305863002 - Excerpt: Submit your resume for future full time openings Cambridge, MA and Durham, NC Company Overview: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases. Not seeing a role that suits you? Send us your resume and we will keep you in mind for future opportunities on the Beam Team! ### Therapeutic Specialist II - Gilead Sciences - Location: China - Shenyang (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Shenyang/Therapeutic-Specialist-I_R0051136-1 - Excerpt: Therapeutic Specialist II China - Shenyang posted: Posted 24 Days Ago ### Senior Therapeutic Specialist - Gilead Sciences - Location: Norway - Oslo (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Norway---Oslo/Senior-Therapeutic-Specialist_R0052304-1 - Excerpt: Senior Therapeutic Specialist Norway - Oslo posted: Posted 30 Days Ago ### Senior Therapeutic Specialist II - Gilead Sciences - Location: China - Tianjin (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Tianjin/Senior-Therapeutic-Specialist-II_R0052081-1 - Excerpt: Senior Therapeutic Specialist II China - Tianjin posted: Posted 30+ Days Ago ### Sr Therapeutic Specialist - HIV - Gilead Sciences - Location: Australia - Sydney (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Australia---Sydney/Sr-Therapeutic-Specialist_R0051369-2 - Excerpt: Sr Therapeutic Specialist - HIV Australia - Sydney posted: Posted 30+ Days Ago ### Sr Therapeutic Specialist (愛知県) - 肝臓領域 - Gilead Sciences - Location: Japan - Tokyo (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Japan---Tokyo/Sr-Therapeutic-Specialist------_R0052840-6 - Excerpt: Sr Therapeutic Specialist (愛知県) - 肝臓領域 Japan - Tokyo posted: Posted Today ### Sr Therapeutic Specialist（関西） - Gilead Sciences - Location: Japan - Tokyo (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Japan---Tokyo/Sr-Therapeutic-Specialist--_R0052782-4 - Excerpt: Sr Therapeutic Specialist（関西） Japan - Tokyo posted: Posted 9 Days Ago --- Source-backed benefit claims include source links; other benefit values are labeled separately.