# FewerJobs export - 100 curated jobs
Generated: 2026-08-10T00:53:21.402Z
Source: https://fewerjobs.com

## Filters applied
- **q**: Summit Therapeutics
- **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**: 2
- **per_page**: 100
- **sort**: relevance

## Jobs
### Senior Director/Executive Director, DMPK - Iambic Therapeutics
- Location: San Diego HQ, San Diego, California, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-13
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.ashbyhq.com/iambic-therapeutics/416f46b9-e8f1-44e7-8749-590ee26e6d52
- Excerpt: Senior Director/Executive Director, DMPK San Diego HQ, San Diego, California, United States JOB SUMMARY Iambic Therapeutics is seeking an experienced DMPK leader to lead our Drug Metabolism & Pharmacokinetics function. Reporting to senior leadership, you will define the scientific strategy for DMPK from early discovery through IND-enabling studies. You will collaborate with internal and external partners to plan and execute DMPK studies. This is a high-impact, hands-on leadership role for someone who thrives at the intersection of rigorous science and strategic drug development. KEY RESPONSIBILITIES - Lead and manage all DMPK strategy and execution across Iambic's discovery programs, setting clear goals and ensuring alignment with cross-functional program teams. - Design and oversee non-clinical ADME/PK studies and PK/PD modeling to enable candidate selection and accelerate IND filings. - Serve as the internal DMPK subject matter expert, partnering with medicinal chemistry, biology, toxicology, and clinical teams to interpret data and guide program decisions. - Build and manage a high-performing network of CRO partners and academic collaborators to supplement internal capabilities. - Lead preparation and review of DMPK sections for regulatory submissions including INDs and NDAs; interact with health authorities as needed. - Champion compliance with ICH guidelines, FDA regulations, and industry best practices across all DMPK activities. - Contribute scientific expertise to business development, due diligence, and partnership evaluations. - Stay at the forefront of emerging DMPK science, technologies, and regulatory trends to continuously strengthen the function. QUALIFICATIONS - PhD in Pharmacokinetics, Pharmaceutical Sciences, or closely related discipline or PharmD - 12+

### Associate Director, Global Drug Substance Commercialization, Critical Raw Materials - Vaxcyte Inc
- Location: San Carlos, California, United States (unspecified)
- Salary: $174K-$203K
- Posted: 2025-11-07
- 401(k) match: listed (not source-backed)
- Apply: https://boards.greenhouse.io/vaxcyte/jobs/4974572008?gh_jid=4974572008
- Excerpt: Associate Director, Global Drug Substance Commercialization, Critical Raw Materials San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: The Associate Director for Drug Substance (DS) Commercialization has the accountability for launch readiness and commercial supply of associated raw materials for production of eCRM and associated components for glycoconjugate vaccines. This role focuses on technical launch planning and execution by bringing best-practices and coordinating cross-functional efforts

### Senior Regulatory Affairs Program Manager - Immunitybio Inc
- Location: Summit, NJ (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-28
- 401(k) match: listed (not source-backed)
- Apply: https://nant.wd5.myworkdayjobs.com/ImmunityBio/job/Summit-NJ/Senior-Regulatory-Affairs-Program--Manager_R2993
- Excerpt: Senior Regulatory Affairs Program Manager Summit, NJ posted: Posted 15 Days Ago

### Specialist III, Regulatory Lifecycle Maintenance - Immunitybio Inc
- Location: Summit, NJ (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://nant.wd5.myworkdayjobs.com/ImmunityBio/job/Summit-NJ/Specialist-III--Regulatory-Lifecycle-Maintenance_R2858
- Excerpt: Specialist III, Regulatory Lifecycle Maintenance Summit, NJ posted: Posted 30+ Days Ago

### Executive Director / Vice President, Corporate and Internal Communications - BioPharma - Dianthus Therapeutics
- Location: Remote (remote)
- Salary: Not disclosed
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/dianthustherapeutics/jobs/4679135005
- Excerpt: Executive Director / Vice President, Corporate and Internal Communications - BioPharma Remote About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology - enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation - enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role BioPharma Experience is required. We are seeking a strategic, creative, and execution-oriented ED / VP, Corporate & Internal Communications to build and lead a modern, high-impact communications function in a fast-growing biotech company. This role sits at the intersection of people, corporate brand, and business strategy-responsible for shaping how we communicate internally and externally, strengthening employee engagement, elevating our corporate brand, and ensuring a consistent and compelling company narrative across all audiences, while operating as predominantly a remote company. You will serve as a trusted advisor to senior leadership and partner closely with the VP of Marketing and VP of Investor Relations to ensure alignment across corporate and internal communications. We are building a culture of individuals who hold our core principles at

### Executive Director, Investor Relations - Entrada Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $292K-$335K
- Posted: 2026-03-12
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/entradatherapeutics/jobs/5077431007
- Excerpt: Executive Director, Investor Relations Boston, MA The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1). 2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670). We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are intellectually curious and can bring new ideas and perspectives to lead the development, implementation, and management of our

### Manager, Reporting and Insights - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Manager--Reporting-and-Insights_Req178468
- Excerpt: Manager, Reporting and Insights SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Financial Advisor - Summit Credit Union - LPL Financial
- Location: Waukesha WI (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://lplfinancial.wd1.myworkdayjobs.com/BD_Partners/job/Waukesha-WI/Financial-Advisor---Summit-Credit-Union_R-049722
- Excerpt: Financial Advisor - Summit Credit Union Waukesha WI posted: Posted 30+ Days Ago

### Senior Counsel, Commercial Legal & Compliance - Compass Therapeutics
- Location: Boston, MA (unspecified)
- Salary: $210K-$290K
- Posted: 2026-03-20
- 401(k) match: 6% (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://www.compasstherapeutics.com/join-us/jobs?gh_jid=5159186008
- Excerpt: Senior Counsel, Commercial Legal & Compliance Boston, MA Compass Therapeutics, Inc. was founded in 2014 and is headquartered in Boston, MA. We are an oncology-focused biopharmaceutical company discovering and developing proprietary antibody-based therapeutics to treat multiple diseases. Our robust pipeline currently includes four clinical assets spanning all phases of development, with novel mechanisms of action, and first-in-class or best-in-class potential across multiple tumor types. Our lead clinical-stage asset, tovecimig, has completed a randomized late-stage biliary tract cancer study and we are preparing for a BLA submission. We are now at an exciting inflection point as we build out a commercial organization to support our first product launch. This is a unique and pivotal moment to join us and help make a meaningful impact on patients' lives. For more information, visit www.compasstherapeutics.com . Position Overview: Our Legal team is seeking a commercially experienced and business-minded Senior Counsel, Commercial Legal & Compliance reporting directly to our General Counsel. This high-impact role will lead the development of our commercial legal and compliance capabilities and framework in preparation for a BLA submission and potential first product launch. This role will partner cross-functionally to enable compliance commercialization while mitigating nuanced legal and regulatory risk specific to the life sciences industry. The ideal candidate is a pragmatic problem-solver who can balance legal rigor with business practicality in a fast-moving environment. We seek candidates who appreciate our unique opportunity to impact patients in need of new therapeutic options. This position is on-site at our office in Brighton,

### Associate Director, Clinical Supply Chain Management - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $170K-$190K
- Posted: 2026-04-02
- 401(k) match: listed (not source-backed)
- 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

### Manufacturing Associate - CAR-T - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Manufacturing-Associate---CAR-T_R1603310
- Excerpt: Manufacturing Associate - CAR-T Summit West - NJ - US posted: Posted Today

### Associate Director, International Marketing Strategy Lead – Acute and Menstrual Migraine - 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 (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013336697-associate-director-international-marketing-strategy-lead-acute-and-menstrual-migraine
- Excerpt: Associate Director, International Marketing Strategy Lead – Acute and Menstrual Migraine 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: Role Summary: The Associate Director, Strategy Lead - Acute and Menstrual Migraine serves as a strategic, cross-functional leader accountable for shaping and aligning the marketing strategy across the Acute and Menstrual Migraine. This role provides leadership and direction to three Sr. Managers overseeing Menstrual Migraine, Acute, and PCP/Digital engagement, ensuring their work is integrated into a cohesive strategy that supports brand objectives, customer needs, and organizational priorities. Key Responsibilities: Lead the overall strategic direction for the Acute and Menstrual Migraine portfolio, ensuring strong alignment across brand, customer, and channel strategies. Prepare for a successful launch strategy for Menstrual Migraine for Aquipta and Ubrelvy. Manage and develop three direct reports Ensure integration of segment-specific plans into a unified portfolio strategy that maximizes reach, impact, and efficiency. Oversee development and execution of marketing initiatives across Acute and Menstrual Migraine, while enabling PCP and digital engagement strategies that strengthen portfolio performance. Translate market insights, customer feedback,

### Senior Electrical Technician - The Procter & Gamble Company
- Location: GREENSBORO BROWN SUMMIT PLANT (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pg.wd5.myworkdayjobs.com/1000/job/GREENSBORO-BROWN-SUMMIT-PLANT/Senior-Electrical-Technician_R000135715
- Excerpt: Senior Electrical Technician GREENSBORO BROWN SUMMIT PLANT posted: Posted 30+ Days Ago

### Lead Engineer, CSV - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-14
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Lead-Engineer--CSV_R1602403
- Excerpt: Lead Engineer, CSV Summit West - NJ - US posted: Posted 29 Days Ago

### Associate Director, Patient Services - Axsome Therapeutics
- Location: New York, NY (unspecified)
- Salary: $155K-$185K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5779343004
- Excerpt: Associate Director, Patient Services New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role Axsome Therapeutics is seeking an Associate Director, Patient Services to lead the establishment and growth of a new Patient Services Hub. This role will work closely with the Director, Patient Services for developing, implementing, and overseeing all aspects of the Hub's operations, ensuring efficient and seamless patient access to therapies and support services. This role requires a strong leader to build and manage the hub team, foster collaborative relationships, and drive continuous improvement within a fast-paced environment. This role will have close collaboration among, and provide ad hoc support to, Field Access and Patient Service functions within the Market Access team, as related to the HUB.

### Director, Global Product Leader - Crinetics Pharmaceuticals INC
- Location: Remote (remote)
- Salary: $187K-$233K
- Posted: 2026-05-23
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Director--Global-Product-Leader_JR000630
- Excerpt: Director, Global Product Leader Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: This position will lead several early or one late-stage development programs and contribute to portfolio strategy for other programs within a growing preclinical and clinical stage pipeline covering endocrinology and endocrine related tumors. The Director, Global Product Leader is responsible for the strategic leadership of a Global Product Team, overseeing strategic planning, decision making, and resource/budget management and prioritization across development, regulatory, CMC, operations, and business functions to ensure rapid, efficient, and successful progression of the program(s). This role will be responsible for the full lifecycle management of their product and ensure that strategic plans and goals are met. The Global Product Leader will ensure cross-functional and organizational readiness for regulatory

### Scientist, Investigations Team - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-09
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Scientist--Investigations-Team_R1603379
- Excerpt: Scientist, Investigations Team Summit West - NJ - US posted: Posted 3 Days Ago

### Senior Corporate Counsel, Contracts (Clinical Development) - Revolution Medicines
- Location: Redwood City, California, United States (unspecified)
- Salary: $244K-$282K
- Posted: 2026-04-10
- 401(k) match: listed (not source-backed)
- Apply: https://www.revmed.com/careers-list/?gh_jid=7695536003
- Excerpt: Senior Corporate Counsel, Contracts (Clinical Development) Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: The Senior Corporate Counsel, Contracts (Clinical Development) will support the Company's clinical research and development activities by drafting, negotiating, and advising on a broad range of clinical and research-related agreements. This role partners closely with Clinical Development, Clinical Operations, Biometrics, Medical Affairs, Procurement, and Legal and Compliance teams to enable efficient and compliant execution of clinical programs. The ideal candidate has strong experience with clinical trial agreements and related contracts in a biotech or pharmaceutical setting, excellent judgment, and the ability to manage multiple priorities in a fast-paced environment. Key responsibilities include: - Draft, review, and negotiate a wide range of clinical development agreements, including: - Clinical Trial Agreements (CTAs). - Site agreements and amendments. - CRO, SMO, and vendor agreements. - Consulting agreements for investigators and key opinion leaders. - Data sharing, biometrics, and lab services agreements. - Advise internal

### Construction Engineering Specialist - Fluor Corporation
- Location: Browns Summit, US-NC, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://careers.fluor.com/careers/job/1099551220576
- Excerpt: Construction Engineering Specialist Browns Summit, US-NC, United States

### Plant Technician - Manufacturing - The Procter & Gamble Company
- Location: GREENSBORO BROWN SUMMIT PLANT (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pg.wd5.myworkdayjobs.com/1000/job/GREENSBORO-BROWN-SUMMIT-PLANT/Plant-Technician---Manufacturing_R000134701
- Excerpt: Plant Technician - Manufacturing GREENSBORO BROWN SUMMIT PLANT posted: Posted 30+ Days Ago

### Sr. Medical Director, Pharmacovigilance - Maplight Therapeutics Inc
- Location: Remote (remote)
- Salary: $319K-$361K
- Posted: 2025-12-09
- Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5025985008
- Excerpt: Sr. Medical Director, Pharmacovigilance Remote Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You'll Do: The Senior Medical Director, Pharmacovigilance will lead the medical safety evaluation and benefit-risk assessment for products throughout their lifecycle with focus on patient well-being and compliance and applicable regulatory requirements. This person will lead cross-functional safety management team (SMT) and collaborate with other members Clinical Development and Medical Affairs (CDMA), contract research organizations (CROs), and drug development collaborators/partners to ensure that all clinical safety and benefit-risk assessment is performed adequately for assigned products. Reporting to the Vice President, Pharmacovigilance, the Senior Medical Director will oversee cross-functional teams and may have direct reports Responsibilities: - Lead product safety surveillance and oversee evolving safety and benefit-risk profiles for assigned products. - Lead cross-functional safety management team (SMT) for assigned products, and responsible for the on-going assessment of benefit-risk profiles and related actions during the product life cycle. - Review safety data from various sources (e.g. pre-clinical, clinical trial data, post-marketing, literature) throughout the development process as well as post marketing for assigned products. - Responsible for conducting signal detection activities, monitoring, evaluation, interpretation and appropriate management and communication of safety information - Represent pharmacovigilance on cross-functional product/project teams including review of safety sections of protocols, investigator brochures, informed

### Associate Director, Clinical Pharmacology - Crinetics Pharmaceuticals INC
- Location: Remote (remote)
- Salary: $166K-$208K
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Associate-Director--Clinical-Pharmacology_JR000603
- Excerpt: Associate Director, Clinical Pharmacology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Associate Director, Clinical Pharmacology will be responsible for developing clinical pharmacology strategy suitable for target product profile (TPP) and clinical development plan (CDP), leading the design, execution, interpretation, and reporting of Phase 1 clinical pharmacology studies, and serve as clinical pharmacology lead on studies and project teams. The work will support projects at various stages of development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance therapeutics for rare endocrine disorders and endocrine-related cancers. This is a unique opportunity to work with a proven and well-funded drug discovery and development team in a small company environment in the heart of

### Manager, Label Operations - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Manager--Label-Operations_R1603062
- Excerpt: Manager, Label Operations Summit West - NJ - US posted: Posted 7 Days Ago

### Financial Advisor - The Summit Federal Credit Union - LPL Financial
- Location: Syracuse, NY (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://lplfinancial.wd1.myworkdayjobs.com/BD_Partners/job/Syracuse-NY/Financial-Advisor---The-Summit-Federal-Credit-Union_R-049905
- Excerpt: Financial Advisor - The Summit Federal Credit Union Syracuse, NY posted: Posted 30+ Days Ago

### Associate Director, Pharmacovigilance - Dianthus Therapeutics
- Location: Remote (remote)
- Salary: Not disclosed
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/dianthustherapeutics/jobs/4691789005
- Excerpt: Associate Director, Pharmacovigilance Remote About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology - enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation - enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role As the Associate Director, Pharmacovigilance, you will work closely with the Safety team to support ongoing clinical trials. This role is critical in ensuring patient safety and regulatory compliance throughout the drug development lifecycle. Day to day, you will work closely with safety physicians, clinical teams, and external stakeholders to manage safety data and contribute to safety oversight. You must have experience reviewing adverse events, safety signals, and coordinate/contribute to the Safety Review Committee (SRC) and Drug Safety Monitoring Boards (DSMB) meetings. You must have experience supporting clinical pharmacovigilance activities and working with DSMBs in order to be successful in this role. This is a unique role that will allow you to work collaboratively with the growing pharmacovigilance team that is working closely with cross functional teams to help Dianthus elevate

### Medical Director Pharmacovigilance - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $285K-$330K
- Posted: 2026-06-01
- 401(k) match: listed (not source-backed)
- 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

### Retail Media Account Executive - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-29
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Retail-Media-Account-Executive_Req182181
- Excerpt: Retail Media Account Executive SMYRNA PACES SUMMIT - 9125 posted: Posted 14 Days Ago

### Director, Clinical Quality Assurance - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $229K-$260K
- Posted: 2026-05-13
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5995887004
- Excerpt: Director, Clinical Quality Assurance Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director of Clinical Quality Assurance (CQA) is a senior member of the CQA team and will lead and perform day-to-day clinical quality operations and compliance activities to support the success of the clinical studies sponsored or supported by Corcept. This is a hybrid role typically requiring on-site presence at least 3 days per week. Responsibilities: - Lead Clinical Quality Assurance activities as line manager to assigned CQA Leads and working with therapeutic area teams to support success of the clinical studies sponsored or supported by Corcept - Champion and influence management and growth of the Clinical Quality Assurance team with the goal of attracting and developing talent, creating a rewarding professional environment, and ensuring that the team's capabilities meet Corcept's future needs - Lead, manage, and train others on GCP audits, including clinical investigative site audits, clinical

### Manager, Advertising Operations (Decor) - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-18
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Manager--Advertising-Operations--Decor-_Req180437
- Excerpt: Manager, Advertising Operations (Decor) SMYRNA PACES SUMMIT - 9125 posted: Posted 25 Days Ago

### Principal Product Leader, Therapeutics Discovery - Genentech, Inc.
- Location: South San Francisco, California, United States of America (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- 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.

### Sr. Analyst, Reporting and Insights - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Sr-Analyst--Reporting-and-Insights_Req178426-1
- Excerpt: Sr. Analyst, Reporting and Insights SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Vice President - Pricing & Market Access - Kymera Therapeutics Inc
- Location: Watertown, MA (unspecified)
- Salary: $315K-$395K
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7770045003#open-positions
- Excerpt: Vice President - Pricing & Market Access Watertown, MA Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn . How we work: - PIONEER : We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. - COLLABORATE : We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. - BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: The Head of Pricing & Market Access will lead global and U.S. pricing, reimbursement, access, and value strategies across Kymera's pipeline and future commercial products. Reporting to the Chief Commercial Officer, this executive will play a critical role in maximizing patient access and commercial

### CDL A Tanker HazMat Driver/Tech - Republic Services
- Location: Browns Summit, NC, USA (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-29
- 401(k) match: listed (not source-backed)
- Apply: https://republic.wd5.myworkdayjobs.com/republic/job/Browns-Summit-NC-USA/HazMat-Driver-Tech---CDL--A-_R-166834
- Excerpt: CDL A Tanker HazMat Driver/Tech Browns Summit, NC, USA posted: Posted 14 Days Ago

### Senior Director, Commercial Manufacturing, Science and Technology - Cogent Biosciences Inc
- Location: Remote, United States (remote)
- Salary: $240K-$280K
- Posted: 2026-05-20
- Parental leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/cogentbiosciences/jobs/4254112009
- Excerpt: Senior Director, Commercial Manufacturing, Science and Technology Remote, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM and PEAK in GIST, including an encouraging safety profile across 600+ patients in single agent and combination dosing. The Role: This position oversees late phase through commercialization small molecule drug product manufacturing at partner Contract Development and Manufacturing Organizations (CDMOs) and ensures high-quality products are delivered on time and within budget. Serve as a technical expert who leads the transfer of manufacturing processes to commercial scale. Manage processes, systems and infrastructure that meet safety, cGMP manufacturing, and regulatory compliance. Provide technical expertise and oversight for process validation, lifecycle management, and continuous improvement. Anticipate and solve complex manufacturing issues. Work in collaboration with internal and external stakeholders including CMC, Quality, Supply Chain and Regulatory, as well as CDMOs. Responsibilities: - Lead commercial drug product CMC lifecycle activities such as post-approval change management, process validation

### Administrative Assistant (Director Level) - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Administrative-Assistant--Director-Level-_Req175506-1
- Excerpt: Administrative Assistant (Director Level) SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Thought Leader Liaison - Mid-Atlantic - Corcept Therapeutics
- Location: Charleston, West Virginia, United States (unspecified)
- Salary: $155K-$205K
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6015530004
- Excerpt: Thought Leader Liaison - Mid-Atlantic Charleston, West Virginia, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . We are seeking a motivated, scientifically strong Thought Leader Liaison (TLL) to expand relationships with key opinion leaders (KOLs) and advance understanding of hypercortisolism across multiple specialties. The TLL plays a critical role in shaping Corcept's external scientific engagement through relationship development with endocrinologists, diabetologists, cardiologists, nephrologists, radiologists, endocrine surgeons, and other relevant specialists. The TLL conducts scientific exchange, gathers clinical insights, identifies speakers and advisors, and collaborates with cross-functional teams including KAMs, CSs, MSLs, Marketing, and Medical Affairs. Responsibilities: Thought Leader Engagement & Scientific Exchange - Identify, establish, and maintain relationships with KOLs - Conduct scientifically rich discussions covering disease-state information, clinical evidence, and product-related topics - Address clinical inquiries and provide scientific resources - Build advocacy and expand awareness of cortisol modulation science Cross-Functional Collaboration - Partner closely with KAMs, MSLs, and Clinical Specialists to

### Wastewater Operator I (3rd Shift) - Republic Services
- Location: Browns Summit, NC, USA (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://republic.wd5.myworkdayjobs.com/republic/job/Browns-Summit-NC-USA/Wastewater-Operator-I_R-171546
- Excerpt: Wastewater Operator I (3rd Shift) Browns Summit, NC, USA posted: Posted 30+ Days Ago

### FEP/EPI Customer Engineer - Applied Materials
- Location: Pyeongtaek-NF Summit,KOR (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://amat.wd1.myworkdayjobs.com/External/job/Pyeongtaek-NF-SummitKOR/FEP-EPI-Customer-Engineer_R2621017
- Excerpt: FEP/EPI Customer Engineer Pyeongtaek-NF Summit,KOR posted: Posted 2 Days Ago

### Senior Patient Recruitment and Retention Lead (CONTRACT) - Entrada Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-19
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/entradatherapeutics/jobs/5141480007
- Excerpt: Senior Patient Recruitment and Retention Lead (CONTRACT) Boston, MA The Organization What's happening at Entrada Therapeutics? Entrada is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary and versatile approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. Our lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy (DMD) who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered with Vertex Pharmaceuticals to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1 (DM1). 2026 represents a catalyst-rich period for Entrada. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51). These programs are complemented by the ongoing clinical progress of our DM1 collaboration with Vertex (VX-670). We are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. The Perfect Addition to Our Team You are a seasoned leader in the pharmaceutical industry who is eager to shape and implement patient

### Senior Medical Director, Oncology - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $298K-$351K
- Posted: 2026-03-06
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5821320004
- Excerpt: Senior Medical Director, Oncology Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . Responsibilities: - Design and implement Phase I to III clinical studies - Develop and participate in the writing and review of protocols, investigator brochures, study reports and other clinical and regulatory documents - Provide scientific oversight for Company operational staff, CROs, and clinical trial sites in all areas related to the therapeutic programs - Act as a clinical subject matter expert for both Company team members and for external contacts related to the assigned therapeutic programs - Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems and final reports - Act to provide medical oversight and safety monitoring for ongoing clinical trials including participation in SAE reporting and serving on the safety committee - Play a key role in the analysis, interpretation and delivery of high-quality clinical data - Interact with

### Scientist, QC Analytical, Cell Therapy - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Scientist--QC-Analytical--Cell-Therapy_R1603316-1
- Excerpt: Scientist, QC Analytical, Cell Therapy Summit West - NJ - US posted: Posted Today

### Associate Patient Materials Operations - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Associate-Patient-Materials-Operations_R1603341
- Excerpt: Associate Patient Materials Operations Summit West - NJ - US posted: Posted 2 Days Ago

### Regional Center Partner (PV, Pharmacovigilance) - Roche Holding AG
- Location: Budapest, Pest, Hungary (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-06
- Apply: https://roche.wd3.myworkdayjobs.com/roche-ext/job/Budapest/Regional-Center-Partner--PV--Pharmacovigilance-_202605-111283-1/apply
- Excerpt: Regional Center Partner (PV, Pharmacovigilance) Budapest, Pest, Hungary Take on the role of a Regional Center Partner in Pharmacovigilance and play a pivotal role in ensuring patient safety and regulatory compliance. Collaborate with global experts, drive process improvements, and lead safety reporting in a dynamic, mission-driven environment. Grow your career with Roche and make a real impact on global healthcare outcomes.

### Manufacturing Associate, Breyanzi, Manufacturing Operations - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Manufacturing-Associate--Breyanzi--Manufacturing-Operations_R1603275
- Excerpt: Manufacturing Associate, Breyanzi, Manufacturing Operations Summit West - NJ - US posted: Posted Yesterday

### Therapist I-1 - Summit BHC
- Location: Peak Behavioral Health (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Apply: https://summitbhc.wd1.myworkdayjobs.com/Summit_BHC/job/Peak-Behavioral-Health/Therapist-I-1_JR124629
- Excerpt: Therapist I-1 Peak Behavioral Health posted: Posted 30+ Days Ago

### Material Handler, Material Kitting - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-20
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Material-Handler--Material-Kitting_R1602552-1
- Excerpt: Material Handler, Material Kitting Summit West - NJ - US posted: Posted 23 Days Ago

### Drug CMC Lead - Atomic
- Location: Remote - US (remote)
- Salary: Not disclosed
- Posted: 2026-06-10
- Apply: https://jobs.ashbyhq.com/atomic/6ead018f-f15e-4f50-a3e2-0a9b771d0255
- Excerpt: Drug CMC Lead Remote - US ABOUT US: Indomo is a clinical stage therapeutics company transforming clinic-based procedures into at-home care via device-enabled therapeutics. Indomo's lead program couples a proven corticosteroid with an innovative intradermal self-injection device to create the first fast-acting at-home solution for inflammatory acne lesions. We are seeking a versatile and experienced CMC Lead to lead our drug development and manufacturing. POSITION OVERVIEW: Reporting to the CEO, you will own and execute the Chemistry, Manufacturing & Controls (CMC) strategy and operations for Indomo's drug and combination product portfolio. This leader will drive the advancement of our lead asset through the NDA regulatory pathway, while effectively coordinating cross-functional efforts to integrate drug formulation, analytical strategy, and manufacturing with the medical device component of Indomo's drug delivery system. This role requires deep expertise in regulatory CMC requirements (especially drug product and formulation development, analytical method development/validation, manufacturing scale-up, and quality/regulatory interfacing for combination products). The ideal candidate will be adept at building robust CMC packages that support clinical milestones and regulatory submissions. This individual must be highly self-motivated, optimization-minded, and collaborative amongst internal stakeholders as well as CDMO's and other external partners as appropriate, with a deep sense of personal ownership of deliverables. KEY RESPONSIBILITIES: CMC Program Leadership - Oversee outsourcing and management of drug substance and drug product development at Indomo's CDMO - including formulation optimization, stability, and compatibility with Indomo's drug delivery system. - Set technical requirements and

### Director, Drug Product Development - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $210K-$235K
- Posted: 2026-01-12
- 401(k) match: listed (not source-backed)
- 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

### Sr. Manager, CTDO Automation - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-26
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Sr-Manager--CTDO-Automation_R1601973-1
- Excerpt: Sr. Manager, CTDO Automation Summit West - NJ - US posted: Posted 17 Days Ago

### Associate, Patient Materials Operations, MSS - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Associate--Patient-Materials-Operations--MSS_R1603383
- Excerpt: Associate, Patient Materials Operations, MSS Summit West - NJ - US posted: Posted Today

### Associate Director, Health Economics & Outcomes Research/Real-World Evidence (HEOR/RWE) - Mineralys Therapeutics Inc
- Location: US Remote (remote)
- Salary: $175K-$200K
- Posted: 2026-06-10
- Apply: https://job-boards.greenhouse.io/mineralystherapeutics/jobs/5253432008
- Excerpt: Associate Director, Health Economics & Outcomes Research/Real-World Evidence (HEOR/RWE) US Remote “Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. For more information, please visit https://mineralystx.com . Follow Mineralys on LinkedIn, Twitter and Bluesky” Mineralys is a fully remote company. Position Summary: The Associate Director, HEOR / Real-World Evidence (RWE) plays a strategic and scientific leadership role in developing and executing evidence strategies that support the clinical and economic value of our innovative therapy. This position is responsible for designing and delivering real-world and outcomes research evidence to support medical affairs, market access, and regulatory objectives. The role focuses on generating high-quality, decision-relevant evidence, including observational studies, external control arms, and economic models, and indirect treatment comparisons, to contextualize clinical outcomes, demonstrate value, and support stakeholder decision- making. The Associate Director collaborates cross-functionally with Medical Affairs, biostatistics, and commercial teams, while also engaging external partners such as academic researchers, key opinion leaders, and data vendors. This role contributes to strategic evidence planning, scientific communication, and advancing real-world data capabilities within a matrixed organization. Key Responsibilities: - Lead the design, execution, and oversight of HEOR and RWE studies, including observational studies (retrospective/prospective cohorts), economic models, external control arms and indirect treatment comparisons. - Oversee data

### Associate Director, Regulatory Strategy - Syndax Pharmaceuticals Inc
- Location: New York, NY (unspecified)
- Salary: $200K-$225K
- Posted: 2026-03-09
- 401(k) match: listed (not source-backed)
- Apply: https://syndax.com/join-us/careers/?gh_jid=5819781004
- Excerpt: Associate Director, Regulatory Strategy New York, NY Syndax Pharmaceuticals is looking for an Associate Director, Regulatory Strategy At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. The Role: The Associate Director, Regulatory Strategy will be responsible for developing and implementing regulatory strategies to secure global investigational and marketing applications for assigned product(s) in the assigned therapeutic area. Leads the Product Regulatory Sub team. Ensures strategic messaging and content of global regulatory dossiers. May serve as the primary regulatory interface with the Asset Strategy Team and sub teams. Proactively anticipates and mitigates regulatory risks. Ensures compliance with global regulatory requirements. Manages assets through all phases of development from pre-FIH through active life cycle management activities. Demonstrates an understanding of drug development and exhibits leadership behaviors consistent with level. Has direct experience with regulatory acceleration strategies, developing regulatory strategy, analyzing regulatory precedence and operational excellence in execution of regulatory strategy. This role may lead a team of regulatory professionals. Key Responsibilities: - Ensure the development and flawless execution of regulatory strategies for the assigned products/projects. - Strategic partner for internal cross functional stakeholders both within and external to the regulatory organization.. - Represents Syndax to regulatory health authorities, e.g. FDA, for all products and businesses. - Lead the preparation of submissions, which may include INDs, Briefing Documents, Orphan Drug Applications, and Marketing Applications, etc. Work

### Manager, Principal Compliance Engineer - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Manager--Principal-Compliance-Engineer_R1598144
- Excerpt: Manager, Principal Compliance Engineer Summit West - NJ - US posted: Posted 30+ Days Ago

### Quality Control Laboratory Analyst - The Procter & Gamble Company
- Location: GREENSBORO BROWN SUMMIT PLANT (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pg.wd5.myworkdayjobs.com/1000/job/GREENSBORO-BROWN-SUMMIT-PLANT/Quality-Control-Laboratory-Analyst_R000135711
- Excerpt: Quality Control Laboratory Analyst GREENSBORO BROWN SUMMIT PLANT posted: Posted 30+ Days Ago

### Head of DMPK - General Proximity
- Location: San Francisco, CA (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-15
- Apply: https://job-boards.greenhouse.io/generalproximity/jobs/5997363004
- Excerpt: Head of DMPK San Francisco, CA tl;dr General Proximity is a seed-stage startup developing the next generation of induced proximity medicines (IPMs). Our OmniTAC drug discovery engine furnishes molecules that co-opt existing cellular machinery to overcome therapeutic challenges, which have remained unapproachable to other modalities for decades. We are seeking a first-rate DMPK expert to help us pioneer this uncharted frontier of drug discovery. Our Story A long-standing challenge in drug discovery is the development of molecules capable of modulating difficult or "undruggable" targets. Disease-causing proteins can be dysfunctional in many different ways, but our armamentarium for fixing them is quite limited. The most common mechanism of action for FDA-approved drugs is inhibition [1] , but there are many other possible perturbation types whose potential remains unrealized. General Proximity is a seed-stage drug discovery company developing a novel platform technology to solve this problem. We make bifunctional drugs that induce the modification of drug targets by existing cellular machinery (rather than through direct modulation by the drug, the classical approach). Historically, the development of technologies that allow one to push new buttons in biology has been an incredibly fertile field for the discovery of new medicines[ 2 , 3 , 4 ], and our technology holds the same promise. The Position We are seeking an experienced Head of DMPK to lead and shape our drug metabolism and pharmacokinetics function. This is a high-impact leadership role in which you will own the DMPK strategy across our small molecule portfolio, build and

### SmartStart Install Automation Engineer - Applied Materials
- Location: Pyeongtaek-NF Summit,KOR (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://amat.wd1.myworkdayjobs.com/External/job/Pyeongtaek-NF-SummitKOR/SPG---SmartStart-Install-Automation-Engineer_R2615882
- Excerpt: SmartStart Install Automation Engineer Pyeongtaek-NF Summit,KOR posted: Posted 30+ Days Ago

### Senior Director, Drug Metabolism and Pharmacokinetics (DMPK) - Nuvalent Inc
- Location: Cambridge, MA / Remote (remote)
- Salary: $270K-$295K
- Posted: 2026-03-24
- Apply: https://boards.greenhouse.io/nuvalent/jobs/5835248004?gh_jid=5835248004
- Excerpt: Senior Director, Drug Metabolism and Pharmacokinetics (DMPK) Cambridge, MA / Remote The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role The Senior Director, DMPK will serve as the company's key expert overseeing DMPK strategy across the entire company, including late-stage discovery, development, NDA submission, and commercial readiness, as well as designing, implementing, and interpreting DMPK studies, ensuring high-quality data and regulatory-ready documentation to support IND, CTA, and NDA filings. As part of a growing biotech organization, the role requires a hands-on, collaborative leader who can build and guide a high-performing team while working cross-functionally to advance a dynamic portfolio. This is a pivotal leadership role in a fast‑growing biotech preparing for its first commercial launch. Responsibilities - Provide scientific leadership for all DMPK activities across discovery, preclinical, and development-stage programs. - Develop and execute DMPK strategies, including ADME, bioanalysis, PK/PD modeling, and in vitro/in vivo metabolism studies. - Serve as the primary DMPK representative on program teams, influencing strategy, timelines, and go/no-go decision‑making. - Evaluate DMPK liabilities and optimization strategies for new chemical entities. - Serve as the DMPK lead on cross‑functional program teams (preclinical, clinical, regulatory, CMC, translational medicine). Study Design & Execution - Oversee design, outsourcing, and interpretation of ADME, PK, TK, and

### Xfinity Sales Professional - Comcast Corporation
- Location: PA - Pittsburgh, 15 Summit Park Dr (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 4 weeks (not source-backed)
- Non-birth-parent leave: 4 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://comcast.wd5.myworkdayjobs.com/Comcast_Careers/job/PA---Pittsburgh-15-Summit-Park-Dr/Xfinity-Sales-Professional_R437253
- Excerpt: Xfinity Sales Professional PA - Pittsburgh, 15 Summit Park Dr posted: Posted 30+ Days Ago

### Endocrine Account Manager - Mountain - BridgeBio Pharma, Inc.
- Location: Remote - USA (remote)
- Salary: $155K-$210K
- Posted: 2026-05-18
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Fertility benefits: yes (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/bridgebio/jobs/5139403007
- Excerpt: Endocrine Account Manager - Mountain Remote - USA Mavericks Wanted When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible. Together we define white space, push boundaries, and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask "why not?" and help reengineer the future of biopharma. At BridgeBio, we value curiosity and experimentation-including the ethical & thoughtful use of AI to improve clarity, speed, and quality of work. What You'll Do The Endocrine Account Manager role is a high-impact position that is critically important to BridgeBio's success. The launch of Encaleret will introduce a first-in-class drug for ADH1, or autosomal dominant hypocalcemia type 1, a rare endocrine disease. They will be patient champions with exceptional business and clinical acumen to execute product launches with sustained excellence. In doing so, they will bring a high sense of urgency, a solution-oriented mindset, and a passion to partner with ADH1 providers and patients. Responsibilities

### Senior Director, Channel Strategy and Patient Support - Apogee Therapeutics Inc
- Location: Remote (remote)
- Salary: $280K-$305K
- Posted: 2026-05-13
- 401(k) match: listed (not source-backed)
- 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

### Senior Account Executive, Retail Media - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-28
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Senior-Account-Executive--Retail-Media_Req181893
- Excerpt: Senior Account Executive, Retail Media SMYRNA PACES SUMMIT - 9125 posted: Posted 15 Days Ago

### Central Operations Head (COH) - Tango Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $187K-$281K
- Posted: 2026-05-08
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/tangotherapeutics/jobs/7726623003
- Excerpt: Central Operations Head (COH) Boston, MA Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer. This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing. The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts. Summary We are seeking a Central Operations Head (COH) to provide strategic leadership across clinical drug supply, Clinical Trial Agreement (CTA), and eTMF management to support global clinical development programs. This role partners cross-functionally with Clinical, Regulatory, Legal, Technical Operations, and Operational Excellence to ensure alignment on trial needs, risk management, and execution priorities. You will oversee end-to-end delivery across trials, define outsourcing and vendor strategies, and ensure performance through KPIs, KRIs, and governance. This role is accountable for driving operational excellence, ensuring inspection readiness, and maintaining compliance with global regulations and internal standards. As a leader, you will build and develop a high-performing team, establish scalable processes and best practices, and foster a culture of accountability, innovation, and continuous improvement in a fast-paced biotech environment. Your role - Provide strategic direction for clinical drug supply management,

### Media Specialist - Orange Apron Media - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Analyst--Advertising-Operations---Orange-Apron-Media_Req171949
- Excerpt: Media Specialist - Orange Apron Media SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Director, Clinical Pharmacology - AbbVie Inc.
- Location: North Chicago, IL, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012916437-director-clinical-pharmacology
- Excerpt: Director, Clinical Pharmacology North Chicago, 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: Purpose Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management, regulatory agencies, and external peers. Leads strategic planning for drug development activities and projects to achieve departmental strategies, goals, and objectives. Utilizes scientific expertise to provide appropriate interpretation of data and relates implications of results to management. Serves as liaison to other departments/divisions for any study/project needs. Influences and strategically manages linkages across businesses and understands the impact of business decisions and solutions. Leads teams within Clinical Pharmacology and Pharmacometrics and accountable for effective performance of the teams. Responsibilities Independently leads Clinical Pharmacology/PK/PD activities and multiple major projects. Assists R&D senior management in the selection of action plans that best meets drug development business objectives. Identifies issues impacting multiple complex projects and leads issue resolution. Conducts risk assessments and leads the function in development of contingency plans. Assures project remains in alignment with strategic objectives. Provides overall timelines to assess portfolio opportunities. Negotiates with

### Senior Manager, Retail Media Sales - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-18
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Senior-Manager--Retail-Media-Sales_Req180329-1
- Excerpt: Senior Manager, Retail Media Sales SMYRNA PACES SUMMIT - 9125 posted: Posted 25 Days Ago

### Non-Technical Project/Program Management - Applied Materials
- Location: Pyeongtaek-NF Summit,KOR (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://amat.wd1.myworkdayjobs.com/External/job/Pyeongtaek-NF-SummitKOR/Non-Technical-Project-Program-Management_R2621585-1
- Excerpt: Non-Technical Project/Program Management Pyeongtaek-NF Summit,KOR posted: Posted Today

### Senior Director, Clinical Development - Dianthus Therapeutics
- Location: Remote (remote)
- Salary: Not disclosed
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/dianthustherapeutics/jobs/4683188005
- Excerpt: Senior Director, Clinical Development Remote About Us We are developing potentially best in class therapies for patients living with severe autoimmune diseases. Our lead antibody, claseprubart (DNTH103), is purposefully engineered with extended half-life, improved potency, and high selectivity for only the active C1s complement protein that drives disease pathology - enabling less frequent and more convenient self-administered subcutaneous injections. Our second clinical candidate, DNTH212 is a first and potentially best in class, bifunctional inhibitor that targets clinically validated and complementary disease modifying mechanisms, Type 1 IFN suppression and B cell modulation - enabling potential for improved clinical outcomes and patient friendly convenient, self-administered subcutaneous injections. To learn more, please visit www.dianthustx.com and follow us on LinkedIn . About the Role The Senior Medical Director, Clinical Development will be the clinical and medical strategic lead of one or more clinical trials for DNTH212. Reporting to the SVP, Clinical Development, you will steer the preparation, review and execution of clinical study synopses and protocols, investigator brochures, and clinical study reports; review SAPs and TLF shells, guide the evaluation of emerging clinical trial data, oversee/guide the data interpretation and data mining, and ensure assigned studies are conducted according to GCPs and SOPs. You will act as a the medical monitor in close collaboration with the CRO medical and clinical monitors, ensure timely recruitment in collaboration with clinical operations, oversee/guide in conducting literature searches and reviews, meta-analyses, and publishing data. You must have experience with Rare Diseases or Rheumatology within the biotechnology or pharmaceutical

### Senior Director, Clinical Pharmacology - Crinetics Pharmaceuticals INC
- Location: Remote (remote)
- Salary: $238K-$297K
- Posted: 2026-06-08
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Senior-Director--Clinical-Pharmacology_JR000637
- Excerpt: Senior Director, Clinical Pharmacology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Director, Clinical Pharmacology will be a key member of the development team, developing clinical pharmacology strategy suitable for target product profile (TPP) and clinical development plan (CDP), leading the design, execution, interpretation and reporting of Phase 1 clinical pharmacology studies, and serve as clinical pharmacology lead on studies and project teams. The work will support projects at various stages of development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance small molecule therapeutics for rare endocrine disorders and endocrine-related cancers. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop clinical pharmacology strategy and related

### Corporate Security Officer (Full Time) - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Corporate-Security-Officer--Full-Time--1st--2nd--and-3rd-Shift-_Req158790
- Excerpt: Corporate Security Officer (Full Time) SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Manager, Developmental Sourcing - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $151K-$177K
- Posted: 2026-04-24
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5981667004
- Excerpt: Manager, Developmental Sourcing Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . We are seeking a dynamic and strategic professional to join our organization as a Sourcing Manager within Clinical Research & Development. In this role, you will lead the development and execution of sourcing strategies, manage a diverse supplier portfolio, and drive continuous improvement across procurement processes. You will work cross-functionally to enhance supplier performance, manage risk, and deliver cost-effective, high-quality solutions aligned with business goals. This role supports Clinical Research & Development teams by leading sourcing activities and vendor negotiations for Corcept's clinical trials. This position requires strong analytical skills, excellent communication, strategic thinking, and a proven ability to build and maintain effective supplier and stakeholder relationships. Key Responsibilities: - Develop and implement sourcing strategies to achieve procurement goals and long-term business objectives - Lead the creation and finalization of Site Clinical Trial Agreements (CTAs), CRO agreements, and Investigator

### HazMat Field Driver/Technician - CDL (A)-1 - Republic Services
- Location: Browns Summit, NC, USA (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-02
- 401(k) match: listed (not source-backed)
- Apply: https://republic.wd5.myworkdayjobs.com/republic/job/Browns-Summit-NC-USA/HazMat-Field-Driver-Technician---CDL--A--1_R-176611
- Excerpt: HazMat Field Driver/Technician - CDL (A)-1 Browns Summit, NC, USA posted: Posted 10 Days Ago

### Director, Regulatory Affairs CMC - Corcept Therapeutics
- Location: Redwood City, California, United States (unspecified)
- Salary: $239K-$281K
- Posted: 2026-02-05
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5795300004
- Excerpt: Director, Regulatory Affairs CMC Redwood City, California, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . Lead the preparation of CMC Regulatory documents from pre-IND to marketing authorization submissions in multiple therapeutic areas, molecules, and regions. This position will lead direct reports in the CMC regulatory team, keep up to date on evolving regulations, and lead regulatory intelligence activities. This is a hybrid role that typically requires on-site presence three days per week. Responsibilities: - Effectively maintain, and motivate a high-performing regulatory CMC team, including developing, coaching, and mentoring diverse, talented, and driven staff - Lead regulatory - CMC intelligence activities - Lead regulatory CMC activities for assigned projects consistent with global regulatory requirements , and company policies and procedures - Provide Regulatory CMC guidance to internal teams and lead cross-functional teams to plan and prepare briefing packages, and CMC sections for INDs, and equivalent IMPD sections for CTAs, NDAs/MAAs and other global submissions

### Manager, Retail Media+ Audience Strategy - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Manager--Retail-Media--Audience-Strategy_Req175455
- Excerpt: Manager, Retail Media+ Audience Strategy SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Principal Scientist, Computational Chemistry - Cogent Biosciences Inc
- Location: Boulder, Colorado, United States (unspecified)
- Salary: $165K-$190K
- Posted: 2026-04-16
- 401(k) match: listed (not source-backed)
- Learning budget: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/cogentbiosciences/jobs/4223530009
- Excerpt: Principal Scientist, Computational Chemistry Boulder, Colorado, United States Who We Are: Cogent Biosciences is a publicly traded biotechnology company focused on developing novel precision therapies to treat a broad range of patients with unmet medical needs. Cogent's lead program, bezuclastinib, is designed to selectively and potently inhibit exon 17 mutations found within the KIT receptor tyrosine kinase, including KIT D816V. KIT D816V is responsible for driving a rare and serious condition called Systemic Mastocytosis, and exon 17 mutations are also found in patients with gastrointestinal stromal tumors (GIST), a type of cancer with strong dependence on oncogenic KIT signaling. Bezuclastinib has exhibited promising initial data across all three trials: APEX in AdvSM, SUMMIT in NonAdvSM, and PEAK in GIST, including an encouraging safety profile across 600+ patients in single-agent and combination dosing. The Role: We are seeking an Experienced Computational Chemist who thrives at the intersection of molecular modeling, data‑driven decision making, and innovative drug design. In this role, you will directly influence discovery programs by generating actionable structure‑based insights, developing predictive models, and partnering with multidisciplinary teams to guide molecular design from hits to optimized leads. This is a full-time, on-site position based at our R&D facility in Boulder, Colorado. Responsibilities: - Apply structure‑based and ligand‑based drug design methods-including docking, protein modeling, and a range of computational techniques-to support projects from hit discovery through lead optimization. - Collaborate with project team members, engaging them in iterative structure‑based drug design cycles to generate hypotheses, evaluate targets, triage hits, and guide

### Manager, Advertising Operations (Emerging Segments) - Home Depot (The)
- Location: SMYRNA PACES SUMMIT - 9125 (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://homedepot.wd5.myworkdayjobs.com/CareerDepot/job/SMYRNA-PACES-SUMMIT---9125/Manager--Advertising-Operations--Emerging-Segments-_Req176133
- Excerpt: Manager, Advertising Operations (Emerging Segments) SMYRNA PACES SUMMIT - 9125 posted: Posted 30+ Days Ago

### Senior Manager, Customer Strategy - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/Senior-Manager--Customer-Strategy_2607046753W-1
- Excerpt: Senior Manager, Customer Strategy North America, United States, New Jersey, Summit posted: Posted Yesterday

### Director, Market Access - DACH - Corcept Therapeutics
- Location: Berlin, Berlin, Germany (unspecified)
- Salary: Not disclosed
- Posted: 2026-04-10
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5920705004
- Excerpt: Director, Market Access - DACH Berlin, Berlin, Germany For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Director, Market Access is responsible for defining and executing the market access, pricing, and reimbursement strategy for Corcept's oncology portfolio in DACH. This role is critical to ensuring timely, sustainable, and compliant patient access through successful navigation of DACH complex access environment, including AMNOG, Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen (IQWiG) Bundesausschuss (G ‑ BA), Statutory Health Insurance (SHI) negotiations, and regional access dynamics. The Director will report to DACH GM and serve as the market access lead for DACH, partnering closely with U.S. Headquarters Market Access, Health Economics and Outcomes Research (HEOR), Medical, Commercial and Legal and Compliance to drive optimal launch readiness, reimbursement outcomes, and long ‑ term access success. Responsibilities: Market Access Strategy & Leadership - Develop and lead the DACH German market access strategy for Corcept's oncology assets across the product lifecycle, from

### Clinical Sales Specialist (CS) - Brooklyn, NY - Corcept Therapeutics
- Location: Brooklyn, New York, United States (unspecified)
- Salary: $140K-$155K
- Posted: 2025-11-10
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5704575004
- Excerpt: Clinical Sales Specialist (CS) - Brooklyn, NY Brooklyn, New York, United States For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The CS is accountable for implementing the sales strategies for approved products consistent with Corcept's compliance standards as well as all applicable legal requirements for those key targeted health care providers and hospital systems within an assigned territory. Responsibilities: - Build and develop professional relationships with influential high prescribers and thought leaders in the territory to enhance Corcept brand and product loyalty - Leverages expertise and knowledge of the therapeutic disease state, the marketplace, applicable competitors, industry, and cross-functional activities/plans to anticipate and effectively manage business opportunities and challenges - Develops and implements effective customer specific territory plans and communicates insights to internal stakeholders - Prioritizes time and effort to ensure optimal coverage of appropriate physician specialists based on opportunity and potential - Plan and participate in education programs and speaker dinner programs - Manage

### Associate Director, QC Technical Services - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Associate-Director--QC-Technical-Services_R1601760
- Excerpt: Associate Director, QC Technical Services Summit West - NJ - US posted: Posted 30+ Days Ago

### Scientist, Research & Development - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/Scientist--Research---Development_2607046675W
- Excerpt: Scientist, Research & Development North America, United States, New Jersey, Summit posted: Posted 2 Days Ago

### Associate Director/Director, Technical Operations - Drug Substance (Small Molecules) - Axsome Therapeutics
- Location: New York, NY (unspecified)
- Salary: $175K-$215K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5980968004
- Excerpt: Associate Director/Director, Technical Operations - Drug Substance (Small Molecules) New York, NY Axsome Therapeutics is a biopharmaceutical company leading a new era in the treatment of central nervous system (CNS) conditions. We deliver scientific breakthroughs by identifying critical gaps in care and develop differentiated products with a focus on novel mechanisms of action that enable meaningful advancements in patient outcomes. Our industry-leading neuroscience portfolio includes FDA-approved treatments for major depressive disorder, excessive daytime sleepiness associated with narcolepsy and obstructive sleep apnea, and migraine, and multiple late-stage development programs addressing a broad range of serious neurological and psychiatric conditions that impact over 150 million people in the United States. Together, we are on a mission to solve some of the brain's biggest problems so patients and their loved ones can flourish. For more information, please visit us at www.axsome.com and follow us on LinkedIn and X . About This Role: Axsome Therapeutics is seeking an Associate Director/Director, Technical Operations - Drug Substance (Small Molecules) to provide technical leadership across the development and commercial lifecycle of small‑molecule drug substance programs. This role is responsible for supporting and overseeing drug substance manufacturing activities, including technology transfer, process validation, continued process verification (CPV), and post‑approval process changes at internal and external manufacturing sites. The successful candidate will serve as a key technical leader within CMC, partnering closely with external CDMOs and internal cross‑functional teams (QA, QC, Regulatory, R&D, and Supply Chain) to ensure robust, compliant, and efficient manufacturing operations. This position reports into senior

### Director, HEOR - Definium Therapeutics
- Location: Remote (remote)
- Salary: $227K-$255K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5984722004
- Excerpt: Director, HEOR Remote Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges. Guided by the recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address the underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today's mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. Together we are moving psychiatry forward-beyond better, into a boundless future. Join us! We are seeking a Director of Health Economics & Outcomes Research (HEOR) to support the development and implementation of innovative and strategically focused value evidence generation activities supporting the clinical development, commercialization, and access of Definium products in therapeutic area of brain health disorders. The candidate is responsible for designing and developing research projects, conducting analysis, reporting and publication of HEOR studies, and providing methodologic input to

### Supplier Excellence Engineer - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-03
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/Supplier-Excellence-Engineer_2607042634W
- Excerpt: Supplier Excellence Engineer North America, United States, New Jersey, Summit posted: Posted 9 Days Ago

### Senior Manager, Thought Leader Programming - Corcept Therapeutics
- Location: Remote (remote)
- Salary: $155K-$205K
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=6018997004
- Excerpt: Senior Manager, Thought Leader Programming Remote For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases. Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com . The Senior Manager, Thought Leader Programming (TLP) is responsible for driving peer-to-peer education, generating actionable insights from thought leaders, and translating those insights into educational and commercial strategy. These three functions distinguish this role from Brand Marketing, Sales, Medical Affairs, and the Thought Leader Liaison team, and define where the position creates unique value for the organization. The position requires a proactive, solutions-oriented approach and the ability to operate effectively in a fast-paced and evolving environment. Responsibilities outlined below are not exhaustive; the individual is expected to identify opportunities to improve strategy, execution, and organizational effectiveness. Responsibilities: Thought Leader Engagement & Strategy - Lead the development and execution of thought leader engagement strategies aligned with brand and disease education objectives - Develop and manage KOL relationships required to support advisory boards, educational content development, speaker programs, and strategic initiatives - Partner

### Senior Specialist, QC Microbiology, Cell Therapy - Bristol Myers Squibb
- Location: Summit West - NJ - US (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Summit-West---NJ---US/Senior-Specialist--QC-Microbiology--Cell-Therapy_R1603220
- Excerpt: Senior Specialist, QC Microbiology, Cell Therapy Summit West - NJ - US posted: Posted Yesterday

### Brand Manager, NEOSTRATA - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/Brand-Manager--NEOSTRATA_2607046457W
- Excerpt: Brand Manager, NEOSTRATA North America, United States, New Jersey, Summit posted: Posted 7 Days Ago

### Director, Statistical Programming - Definium Therapeutics
- Location: Remote (remote)
- Salary: $217K-$241K
- Posted: 2026-06-04
- Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5848374004
- Excerpt: Director, Statistical Programming Remote Definium Therapeutics is a late-stage clinical biopharmaceutical company and our mission is to forge a new era of psychiatry by applying scientific rigor to psychedelics, with the goal of developing accessible treatments that unlock healing at scale. Our lead product candidate, lysergide tartrate (our proprietary orally disintegrating tablet form of lysergide (LSD) D-tartrate), represents a highly differentiated, potential best-in-class opportunity for patients suffering from generalized anxiety, major depressive disorder, and posttraumatic stress disorder. Our early stage pipeline includes DT402, the R-enantiomer of MDMA and is under development to target the core symptoms of autism spectrum disorder (ASD), specifically addressing social communication challenges. Guided by the recognition that patients deserve more than better, Definium is relentlessly advancing a new generation of therapeutics intended to address the underlying causes of psychiatric and neurological disorders. By turning evidence into impact, Definium aims to change the trajectory of today's mental health care crisis and enable a healthier future. Headquartered in New York, Definium Therapeutics trades on Nasdaq under the symbol DFTX. Together we are moving psychiatry forward-beyond better, into a boundless future. Join us! As Director, Statistical Programming, this person will provide statistical programming leadership to support analysis and reporting for assigned clinical programs, as well as to support pipeline compounds' regulatory filing and commercialization. Reporting to Vice President, Head of Biometrics and Data Science, this person will lead a group of Statistical Programmers to deliver while also being hands-on. This individual will work closely with biostatisticians for data analysis,

### Director, Biostatistics - Tango Therapeutics Inc
- Location: Boston, MA (unspecified)
- Salary: $191K-$287K
- Posted: 2026-05-08
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/tangotherapeutics/jobs/7728858003
- Excerpt: Director, Biostatistics Boston, MA Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer. Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer. This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing. The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts. Summary In this new role, reporting to the Vice President, Biometrics you will be working with cross‑functional clinical teams responsible for statistical activities across Tango's clinical programs, including overseeing statistical deliverables outsourced to clinical CROs. This is an exciting opportunity to make an impact in the development of transformative therapies that may change patients' lives. You will be a good communicator, collaborative, self-motivated, and forward‑thinking. Your Role: - You will serve as a biostatistics expert for Tango's clinical programs - Provide strategic input to optimize trial designs in early phase dose escalation studies and late phase registrational studies - As a biostatistics representative, proactively collaborate with internal and external CRO team members to coordinate the planning and execution of statistical deliverables - Conduct statistical modeling to enable robust and efficient statistical designs and address identified or potential statistical issues

### US Payroll Supervisor - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/US-Payroll-Supervisor_2607046381W
- Excerpt: US Payroll Supervisor North America, United States, New Jersey, Summit posted: Posted 7 Days Ago

### Senior Scientist Product Development - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/Senior-Scientist-Product-Development_2607045254W
- Excerpt: Senior Scientist Product Development North America, United States, New Jersey, Summit posted: Posted Today

### Associate Director, Strategic Engagement (Thought Leader Liaison), Mid-Atlantic - Mirum Pharmaceuticals Inc
- Location: US Remote (remote)
- Salary: Not disclosed
- Posted: 2026-05-27
- Apply: https://job-boards.greenhouse.io/mirumpharmaceuticals/jobs/5145629007
- Excerpt: Associate Director, Strategic Engagement (Thought Leader Liaison), Mid-Atlantic US Remote MISSION Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases. We are passionate about advancing scientific discoveries to become important medicines for rare disease patients. We are collaborative, creative, and experienced professionals and we're looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously. POSITION SUMMARY The Associate Director, Strategic Engagement also known as Thought Leader Liaison (TLL) serves as a key strategic partner between Mirum Pharmaceuticals and the healthcare community, focusing on cultivating and maintaining relationships with key opinion leaders (KOLs), thought leaders, and other external stakeholders. This role is responsible for building scientific credibility, supporting brand strategy, and ensuring aligned, compliant engagement with external experts to enhance awareness and education. Area of focus will largely be supporting the Hepatology and Gastroenterology community supporting our existing and future products in Alagille, PFIC, PBC, PSC and Hepatitis D. States likely to be included in territory include: PA, DE, VA, MD, DC, WV, OH, KY, MI JOB FUNCTIONS/RESPONSIBILITIES - Develop and communicate the strategic vision and operational plan for engaging KOLs. - Develop and oversee development and execution of individual KOL Mapping KOLs plans. - Partner closely with the Director, Marketing - KOL Strategy and Congress Planning to ensure alignment. - Build and maintain productive, collaborative, and compliant relationships with peers leading teams in Marketing, Market Access, Patient Services, and Medical Affairs. - Work

### Senior Project Manager, Personal Care - The Procter & Gamble Company
- Location: GREENSBORO BROWN SUMMIT PLANT (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pg.wd5.myworkdayjobs.com/1000/job/GREENSBORO-BROWN-SUMMIT-PLANT/Senior-Project-Manager--Personal-Care_R000147632
- Excerpt: Senior Project Manager, Personal Care GREENSBORO BROWN SUMMIT PLANT posted: Posted 30+ Days Ago

### Senior Manager, Clinical Statistical Programmer - Compass Therapeutics
- Location: Boston, MA (unspecified)
- Salary: $140K-$198K
- Posted: 2026-04-08
- 401(k) match: 6% (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://www.compasstherapeutics.com/join-us/jobs?gh_jid=5180839008
- Excerpt: Senior Manager, Clinical Statistical Programmer Boston, MA Compass Therapeutics, Inc. was founded in 2014 and is headquartered in Boston, MA. We are an oncology-focused biopharmaceutical company discovering and developing proprietary antibody-based therapeutics to treat multiple diseases. Our robust pipeline currently includes four clinical assets spanning all phases of development, with novel mechanisms of action, and first-in-class or best-in-class potential across multiple tumor types. Our lead clinical-stage asset, tovecimig, has completed a randomized late-stage biliary tract cancer study and we are preparing for a BLA submission. We are now at an exciting inflection point as we scale our organization to support our first product launch. This is a unique and pivotal moment to join us and help make a meaningful impact on patients' lives. For more information, visit www.compasstherapeutics.com . Our Clinical team is seeking a hands‑on strategic Senior Manager, Clinical Statistical Programmer, reporting to our Director of Biostatistics. The ideal candidate will have a proven track record of successfully leading clinical safety analysis and programming across multiple programs, in a fast-paced environment. This role combines deep technical expertise in SAS and R with ownership of ongoing safety maintenance and leadership in modern data visualization platforms. The individual will support active trials, long‑term safety monitoring, and the integration of complex data streams, including translational and real-world data (RWD). This position works onsite 4 days/week in the Brighton, MA office . Responsibilities Lead Statistical Programming processes, support Clinical strategies, and manage the execution of programming activities across all of our clinical-stage antibody

### Senior Associate Scientist (Contract), Drug Product Analytics - Vaxcyte Inc
- Location: San Carlos, California, United States (unspecified)
- Salary: $56-$62/hr
- Posted: 2026-03-23
- 401(k) match: listed (not source-backed)
- Apply: https://boards.greenhouse.io/vaxcyte/jobs/5154315008?gh_jid=5154315008
- Excerpt: Senior Associate Scientist (Contract), Drug Product Analytics San Carlos, California, United States Join our Mission to Protect Humankind! Vaxcyte is a clinical-stage vaccine innovation company engineering high-fidelity vaccines to protect humankind from the consequences of bacterial diseases, which have serious and costly health consequences when left unchecked. Working to eradicate or treat bacterial infections such as invasive pneumococcal disease, Group A Strep, and Shigella is just the beginning. Our path to success is clear and well-defined, and Vaxcyte is set up to go the distance. WHAT we do is every bit as important as HOW we do it! Our work together is guided by four enduring core values: *RETHINK CONVENTION: We bring creative and intellectual diversity to every facet of the work we do in order to innovate and re-innovate the way vaccines are delivered. *AIM HIGH: We embody our collectively audacious goal to courageously make the most complex biologics ever attempted to protect humankind. *LEAD WITH HEART: Everyone leads at Vaxcyte with a kindness-first, inclusive approach to collaboration and vigorous debate that advances our business objectives. *MODEL EXCELLENCE: The magnitude of our challenge requires our shared commitment to demonstrating integrity, accountability, equality and clarity across communications and decision making. Summary: Vaxcyte is looking for an energetic and talented individual to join our Drug Product Development team. The candidate must have knowledge of and practical experience in analyzing and characterizing biomolecules (proteins, polysaccharide conjugates, vaccines) using a variety of methods, especially immunoassays and multiplexed immunoassay formats. Experience in analyzing vaccine

### Demand Planning Business Lead - Kenvue
- Location: North America, United States, New Jersey, Summit (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://kenvue.wd5.myworkdayjobs.com/kenvue/job/North-America-United-States-New-Jersey-Summit/Demand-Planning-Business-Lead_2607046713W
- Excerpt: Demand Planning Business Lead North America, United States, New Jersey, Summit posted: Posted Yesterday

### Senior Director, Global Regulatory Lead - Immunome Inc
- Location: US Remote (remote)
- Salary: $226K-$270K
- Posted: 2025-11-13
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/immunomeinc/jobs/4982640008
- Excerpt: Senior Director, Global Regulatory Lead US Remote Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been submitted to the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-3050, an IND-cleared FAP-targeted radiotherapy; and IM-1617, an IND-cleared solid tumor ADC. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets. Position Overview As the Global Regulatory Lead at Immunome, you will be the key decision-maker responsible for the development and execution of innovative global regulatory strategies for our therapeutic portfolio to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects. You will work collaboratively across teams to ensure compliance and alignment with corporate objectives, driving the regulatory success of our products in development and throughout their life cycle. This position will report to the Vice President, Regulatory Affairs. Responsibilities Regulatory Strategy Development - Define and implement global regulatory strategies that adapt to changing regulatory and business needs. Cross-Functional Leadership - Communicate key developments to project teams and stakeholders, ensuring alignment and sound judgment. - Anticipate risks and devise solutions, understanding the likelihood of technical success for proposed strategies. Team Leadership - Lead the Global Regulatory Team, fostering a high-performance culture

### CDL A Tanker HazMat Industrial Services Driver/Tech - Republic Services
- Location: Browns Summit, NC, USA (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://republic.wd5.myworkdayjobs.com/republic/job/Browns-Summit-NC-USA/HazMat-Industrial-Services-Driver-Tech---CDL--A-_R-165321-1
- Excerpt: CDL A Tanker HazMat Industrial Services Driver/Tech Browns Summit, NC, USA posted: Posted 30+ Days Ago

### Ion Implant(VSE) Customer Engineer - Applied Materials
- Location: Pyeongtaek-NF Summit,KOR (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://amat.wd1.myworkdayjobs.com/External/job/Pyeongtaek-NF-SummitKOR/Ion-Implant-VSE--Customer-Engineer_R2519323-1
- Excerpt: Ion Implant(VSE) Customer Engineer Pyeongtaek-NF Summit,KOR posted: Posted 30+ Days Ago

### Senior Specialist, Clinical Business Operations - Maplight Therapeutics Inc
- Location: Burlington, MA (unspecified)
- Salary: $115K-$135K
- Posted: 2026-05-05
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/maplighttherapeutics/jobs/5210932008
- Excerpt: Senior Specialist, Clinical Business Operations Burlington, MA Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms. What You'll Do: MapLight is looking for a dynamic and experienced Senior Specialist, Clinical Business Operations. Reporting to the Executive Director, Clinical Operations, the Senior Specialist will be responsible for supporting all aspects of clinical business operations, including vendor selection, contracts, budget management and performance metrics. The ideal candidate will streamline operational procedures across multiple projects to improve timelines and organization of data. Responsibilities: - Vendor selection; including review and analysis, budget negotiations, development, and execution. - Manage the Request for Proposal (RFP) process. This includes: - Work with Clinical Trial Managers (CTM) and Clinical Scientific Leads to develop outsourcing strategy including range of vendors and timelines for award (i.e. schedule a vendor outsourcing strategy meeting). - Use the RFP template to customize to each study. - Create a draft of the RFP for review by the study team. - Communicate with vendors the RFP timelines and milestones and coordinate feedback to questions/answers. - Maintain the internal RFP timelines and milestones. - Following award, be the point of contact to receive the scope of work and budget grid from vendor. - Coordinate the review and consolidate the internal study team's (and finance) questions and comments regarding the

### Director, Clinical Data and Systems - Kymera Therapeutics Inc
- Location: Watertown, MA (unspecified)
- Salary: $195K-$275K
- Posted: 2026-03-05
- 401(k) match: listed (not source-backed)
- Apply: https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7653638003#open-positions
- Excerpt: Director, Clinical Data and Systems Watertown, MA Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn . How we work: - PIONEER : We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. - COLLABORATE : We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. - BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: - Serve as clinical study team Subject Matter Expert for eCOA, IRT, Data Visualization and other clinical data systems. - Lead clinical technologies including planning, execution, and delivery of the clinical data activities on eCOA, IRT and other clinical technologies, implementing standard procedures to initiate best

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