# FewerJobs export - 100 curated jobs Generated: 2026-08-22T16:02:25.680Z Source: https://fewerjobs.com ## Filters applied - **q**: Capricor 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**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Security Analyst - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://jobs.lever.co/capricor/47a257c7-2b7d-4997-9857-5412f5b0eae7 - Excerpt: Security Analyst San Diego, CA ### Process Development Scientist - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://jobs.lever.co/capricor/a9c5bb04-8927-47e6-afd1-0541ce519bc9 - Excerpt: Process Development Scientist San Diego, CA ### Senior Systems Engineer - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/54114b7b-8a41-4828-94aa-8a700323bd33 - Excerpt: Senior Systems Engineer San Diego, CA ### Operations Coordinator - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/9529613a-6d12-4f3b-8006-6aad4813db66 - Excerpt: Operations Coordinator San Diego, CA ### Warehouse Supervisor - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/b933f7b0-0f66-4ebc-aa18-6fc9fdc0761b - Excerpt: Warehouse Supervisor San Diego, CA ### Quality Assurance Associate II - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/7a6b869f-2b42-4e9e-a40f-5ba89d556a12 - Excerpt: Quality Assurance Associate II San Diego, CA ### Facilities Manager - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/be263057-5f3f-4b5b-82d2-126105df191a - Excerpt: Facilities Manager San Diego, CA ### Manager / Senior Manager, Commercial Logistics - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/d27ce56f-4be7-403f-be88-b4f91f41f1a6 - Excerpt: Manager / Senior Manager, Commercial Logistics San Diego, CA ### Animal Technician, Preclinical Studies - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://jobs.lever.co/capricor/34891bd1-ef74-4d19-b96d-d82de3217958 - Excerpt: Animal Technician, Preclinical Studies San Diego, CA ### Process Development Scientist - Bioreactor - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Apply: https://jobs.lever.co/capricor/3f821dc9-67e4-40a0-a929-4efa3162014d - Excerpt: Process Development Scientist - Bioreactor San Diego, CA ### License Associate III - Capricor Therapeutics - Location: Remote (remote) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/0e395722-8f55-4066-80bf-4113d7a1545b - Excerpt: License Associate III Remote ### Director, Quality Assurance & Quality Systems - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/74178259-e3ca-4929-80ec-9dcd8bd3a73b - Excerpt: Director, Quality Assurance & Quality Systems San Diego, CA ### Associate Director / Director of Patient Advocacy - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/73ecaa38-e3c4-44d7-a953-086881f7cc6c - Excerpt: Associate Director / Director of Patient Advocacy San Diego, CA ### Facilities Associate II / III - Capricor Therapeutics - Location: San Diego, CA (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - Apply: https://jobs.lever.co/capricor/4ed96738-2b9e-4b4a-a0c2-325bf757d2c0 - Excerpt: Facilities Associate II / III San Diego, CA ### 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 ### Drug Safety Manager - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-03-19 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4014908 - Excerpt: Drug Safety Manager Viking Therapeutics, Inc. Drug Safety Manager ### Clinical Trial Manager - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-05-11 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/3913773 - Excerpt: Clinical Trial Manager Viking Therapeutics, Inc. Clinical Trial Manager ### Associate Director, Formulation Development - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4079847 - Excerpt: Associate Director, Formulation Development Viking Therapeutics, Inc. Associate Director, Formulation Development ### Director of Process Validation - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-09 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4075036 - Excerpt: Director of Process Validation Viking Therapeutics, Inc. Director of Process Validation ### Senior Director, Marketing - Definium Therapeutics - Location: Remote (remote) - Salary: $252K-$295K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5985751004 - Excerpt: Senior Director, Marketing 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! Definium Therapeutics, formerly known as Mind Medicine, is a clinical stage biopharmaceutical company developing novel product candidates to treat brain health disorders. Our mission is to be the global leader in the development and delivery of treatments that unlock new opportunities to improve patient outcomes. We are developing a pipeline of innovative product candidates, with and without acute perceptual effects, targeting neurotransmitter pathways that play key ### Medical Science Liaison Director/Lead - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-27 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4116882 - Excerpt: Medical Science Liaison Director/Lead Viking Therapeutics, Inc. Medical Science Liaison Director/Lead ### Senior Director, Clinical Development - Definium Therapeutics - Location: Remote (remote) - Salary: $248K-$299K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5808053004 - Excerpt: Senior Director, Clinical Development 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! The Sr. Director, Clinical Development will play a key role in the design and execution of ongoing and new clinical studies and contribute to the clinical development plan for one or more programs. The position will successfully lead and/or serve as the clinical science representative on one or more clinical studies (US and/or global) to deliver high quality data for registration. The position requires the ### Associate Director, Clinical Development - Definium Therapeutics - Location: Remote (remote) - Salary: $170K-$192K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5977186004 - Excerpt: Associate Director, Clinical Development 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! The Associate Director, Clinical Development plays a key role in the design and execution of ongoing and new clinical development studies. This position serves as the clinical science representative on one or more U.S. and/or global clinical studies and contributes to the delivery of high‑quality clinical data to support registration and launch. The role partners cross‑functionally with Clinical Operations, Clinical Pharmacology, Regulatory Affairs, Early Development, ### Senior Director/Vice President, Patient, HCP, and Payer Marketing - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $180K-$280K - Posted: 2026-04-21 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8515720002 - Excerpt: Senior Director/Vice President, Patient, HCP, and Payer Marketing New York, NY Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As a Senior Director / Vice President of HCP and Payer Marketing, you will shape the overall marketing strategy for near-term launch products and build a best in class marketing organization to execute that vision. You and your team will define the brand strategy and create the narrative and materials that drive behavior ### Senior Clinical Trial Associate - Rapport Therapeutics Inc - Location: 99 High Street, Suite 2100 , Boston, MA 02110 (unspecified) - Salary: $90K-$110K - Posted: 2026-04-22 - Apply: https://www.rapportrx.com/careers-board/?gh_jid=5001441007 - Excerpt: Senior Clinical Trial Associate 99 High Street, Suite 2100 , Boston, MA 02110 When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we're driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we're doing this with extraordinary science and awesome people (affectionately called Rapptors). Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies. We are excited about the potential of our lead program, RAP-219. Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder. The strength of Rapport comes from our Rapptors - who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you're as excited about this opportunity as we are! Your impact: As a Senior Clinical Trial Associate, you'll be a key player in keeping our clinical studies on track-managing the details, supporting the team, and helping bring innovative treatments to patients Your day-to-day: - Coordinates and tracks the distribution and subsequent retrieval of clinical documents, including but not limited to ### Senior Director/VP, Medical Affairs - Click Therapeutics - Location: New York, NY, Boston, MA or Remote (remote) - Salary: $180K-$280K - Posted: 2026-04-29 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8525471002 - Excerpt: Senior Director/VP, Medical Affairs New York, NY, Boston, MA or Remote Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As the Senior Director / Vice President of Medical Affairs, you will be the scientific heartbeat of the organization. You will act as the scientific authority for CT-155. This team generates the evidence (RWE/OLE) needed to prove clinical value and economic impact, supplying the "raw material" that Marketing and Access teams leverage. The ### Senior Director/Vice President, Market Access - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $180K-$280K - Posted: 2026-04-21 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8515744002 - Excerpt: Senior Director/Vice President, Market Access New York, NY Who We Are : Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As a Senior Director / Vice President of Market Access, you will be the backbone of the commercial organization. You will design the financial architecture of the product, shape the external policy and regulatory environments to support PDTs, and ensure long term viability of the PDT category. The role reports to the Chief Commercial Officer and ### Senior Director, Product Marketing - Atricure - Location: Mason, OH; Minnetonka, MN (unspecified) - Salary: $200K-$275K - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/atricure/jobs/4281191009 - Excerpt: Senior Director, Product Marketing Mason, OH; Minnetonka, MN AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure's Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure's Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure's cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure. We foster a culture of inclusion by embracing diverse experiences and individuals where everyone's authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally. POSITION SUMMARY: The Senior Director, Product Marketing is responsible for owning and advancing the overall strategy, growth, and performance of the Pain Management portfolio. This role leads the business case for sustained portfolio growth, owns enterprise ‑ level portfolio and lifecycle strategy, and drives both upstream innovation and downstream commercialization initiatives across the pain management therapy area. The position serves as the primary voice and champion for Pain Management, shaping the long ### Group Manager, Product Marketing - Atricure - Location: Mason, OH; Minnetonka, MN (unspecified) - Salary: $145K-$180K - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/atricure/jobs/4281160009 - Excerpt: Group Manager, Product Marketing Mason, OH; Minnetonka, MN AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure's Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure's AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure's Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure's cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure. We foster a culture of inclusion by embracing diverse experiences and individuals where everyone's authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally. POSITION SUMMARY: The Group Marketing Manager - Pain Management will play a pivotal role in driving the success of the Pain Management franchise by leading both upstream and downstream marketing initiatives for the cardiothoracic application of Cryo Nerve Block . This position will be responsible for shaping therapy's strategic direction, guiding product and procedure development, and ensuring effective market adoption and growth. The role will lead upstream efforts including therapy development, market ### Patient and Community Educators - Southeast - Cogent Biosciences Inc - Location: Remote, United States (remote) - Salary: $190K-$225K - Posted: 2026-04-07 - 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/4210405009 - Excerpt: Patient and Community Educators - Southeast 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: The Patient and Community Educator (PACE) serves as a trusted resource for individuals living with Systemic Mastocytosis (SM) and Gastrointestinal Stromal Tumor (GIST) , as well as their caregivers and community members. Reporting to the Director, Patient and Community Educators, this field-based role is responsible for delivering clear, compassionate, and compliant disease and treatment education through live and virtual engagements. The PACE team will play a critical role in empowering patients and caregivers with knowledge that helps them better understand their condition, navigate their treatment journey, and engage more confidently in conversations with their healthcare teams. This role requires a unique combination of clinical fluency, emotional intelligence, and communication expertise. The ideal candidate is ### Director, Regulatory Strategy - Rapport Therapeutics Inc - Location: 99 High Street, Suite 2100 , Boston, MA 02110 (unspecified) - Salary: $220K-$240K - Posted: 2026-01-24 - Apply: https://www.rapportrx.com/careers-board/?gh_jid=5001273007 - Excerpt: Director, Regulatory Strategy 99 High Street, Suite 2100 , Boston, MA 02110 When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we're driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we're doing this with extraordinary science and awesome people (affectionately called Rapptors). Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies. We are excited about the potential of our lead program, RAP-219. Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder. The strength of Rapport comes from our Rapptors - who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you're as excited about this opportunity as we are! Your Impact: The Director of Regulatory Strategy will play a pivotal role in leading strategic regulatory initiatives for assigned drug development programs. Your Day-to-Day: - Create and implement innovative and effective regulatory strategies to support the development of Rapport global drug development programs - Provide regulatory expertise and advise to cross-functional team ### Senior/Executive Director, Health Economics & Outcomes Research (HEOR) - Viking Therapeutics - Location: Viking Therapeutics, Inc. (unspecified) - Salary: Not disclosed - Posted: 2026-04-29 - Apply: https://recruiting.paylocity.com/Recruiting/Jobs/Details/4127771 - Excerpt: Senior/Executive Director, Health Economics & Outcomes Research (HEOR) Viking Therapeutics, Inc. Senior/Executive Director, Health Economics & Outcomes Research (HEOR) ### Key Account Manager (KAM) - Germany - Corcept Therapeutics - Location: Berlin, Berlin, Germany (unspecified) - Salary: Not disclosed - Posted: 2026-04-13 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5815783004 - Excerpt: Key Account Manager (KAM) - Germany 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 . We are seeking a Key Account Manager (KAM) - Oncology to support the launch and growth of Corcept's oncology portfolio in Germany. This is a unique opportunity to join a pioneering organization as it expands its oncology presence in the European market. The Key Account Manager is responsible for driving awareness, adoption, and appropriate use of Corcept's oncology products within assigned key accounts across Germany. The role focuses on strategic account management, stakeholder engagement, and compliant promotional activities to ensure optimal patient access in a complex healthcare environment. Key Responsibilities: - Develop and execute account based strategic plans tailored to the needs of oncologists, multidisciplinary care teams, hospital systems, and other relevant stakeholders - Achieve sales and performance objectives through high-quality, compliant interactions with healthcare professionals and key decision makers within oncology accounts - Provide accurate, balanced, and ### Therapeutic Mentor - Centerstone - Location: Bradenton, Florida (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Apply: https://centerstone.wd5.myworkdayjobs.com/CenterstoneCareers/job/Bradenton-Florida/Therapeutic-Mentor_JR-030233 - Excerpt: Therapeutic Mentor Bradenton, Florida posted: Posted 2 Days Ago ### Regional Strategic Sales Director - Great Lakes - Heartflow INC - Location: Chicago, IL; Detroit, MI; Indianapolis, IN; Columbus, OH; Cleveland, OH (unspecified) - Salary: $150K-$330K - Posted: 2026-03-27 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/heartflowinc/jobs/5839643004 - Excerpt: Regional Strategic Sales Director - Great Lakes Chicago, IL; Detroit, MI; Indianapolis, IN; Columbus, OH; Cleveland, OH Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFR CT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMap™Analysis), assess coronary blood flow (FFR CT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). Our pipeline of products is growing and so is our team; join us in helping to revolutionize precision heartcare. Heartflow is a publicly traded company (HTFL) that has received international recognition for exceptional strides in healthcare innovation, is supported by medical societies around the world, cleared for use in the US, UK, Europe, Japan and Canada, and has been used for more than 500,000 patients worldwide. The Regional Strategic Sales Director (RSD) is a high-impact leadership role responsible for the strategic expansion, and long-term adoption of Heartflow's portfolio.The RSD will focus on high-level C-suite engagement, CV service line optimization, and scaling Heartflow's full suite of solutions across the region. For FY26, the immediate priority is the successful launch of PCI Navigator - Heartflow's new pre-procedural planning solution for Percutaneous Coronary ### Vice President, Commercial Manufacturing Operations - VERA Therapeutics INC - Location: Remote (remote) - Salary: $248K-$375K - Posted: 2026-06-07 - Apply: https://job-boards.greenhouse.io/veratherapeuticsinc/jobs/4273981009 - Excerpt: Vice President, Commercial Manufacturing Operations Remote Vera Therapeutics is a biotechnology company focused on developing treatments for serious immunological diseases. Vera Therapeutics' mission is to advance treatments that target the source of disease in order to change the standard of care for patients. Vera Therapeutics' lead product candidate is atacicept, a fusion protein self-administered at home as a subcutaneous once weekly injection that blocks both B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), which stimulate B cells to produce autoantibodies contributing to certain autoimmune diseases, including IgA nephropathy (IgAN) and lupus nephritis. Beyond IgAN, Vera Therapeutics is evaluating additional diseases where the reduction of autoantibodies by atacicept may prove clinically meaningful. In addition, Vera Therapeutics holds an exclusive license agreement with Stanford University for a novel, next generation fusion protein targeting BAFF and APRIL, known as VT-109, with wide therapeutic potential across the spectrum of B-cell-mediated diseases. Vera Therapeutics is also evaluating the development of MAU868, a monoclonal antibody designed to neutralize infection with BK virus, which can have devastating consequences in kidney transplant recipients. Vera Therapeutics retains all global developmental and commercial rights to atacicept, VT-109, and MAU868. For more information, please visit www.veratx.com . Our values are the cornerstone of our culture. Our values inspire us every day and guide everything we do-from how we hire great people, to advancing our mission together, to achieving our ultimate goal to improve medical treatment for patients suffering from immunological diseases. Position Summary: The Vice President, Manufacturing Operations will report ### Therapeutic Specialist - Gilead Sciences - Location: Spain - Alicante (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Spain---Alicante/Therapeutic-Specialist_R0052600 - Excerpt: Therapeutic Specialist Spain - Alicante posted: Posted 2 Days Ago ### Therapeutic Specialist I - Gilead Sciences - Location: China - Kunming (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Kunming/Therapeutic-Specialist-I_R0052372-2 - Excerpt: Therapeutic Specialist I China - Kunming posted: Posted 30+ Days Ago ### (Senior) Medical Director, Medical Science - Rapport Therapeutics Inc - Location: 99 High Street, Suite 2100 , Boston, MA 02110 (unspecified) - Salary: $250K-$295K - Posted: 2026-05-20 - Apply: https://www.rapportrx.com/careers-board/?gh_jid=5001260007 - Excerpt: (Senior) Medical Director, Medical Science 99 High Street, Suite 2100 , Boston, MA 02110 When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we're driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we're doing this with extraordinary science and awesome people (affectionately called Rapptors). Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies. We are excited about the potential of our lead program, RAP-219. Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder. The strength of Rapport comes from our Rapptors - who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you're as excited about this opportunity as we are! Your Impact: This Medical Director role offers the opportunity to partner closely with cross-functional leaders to support both clinical development and strategic initiatives in support of the RAP-219 Epilepsy program. The position provides broad exposure to multiple programs, with the chance to work hands-on in the details while growing within ### Therapeutic Specialist II - Gilead Sciences - Location: China - Shenyang (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Shenyang/Therapeutic-Specialist-I_R0051136-1 - Excerpt: Therapeutic Specialist II China - Shenyang posted: Posted 24 Days Ago ### Design Assurance CAPA Manager - Cardiac Rhythm Management and Diagnostics (CRMDx) - Boston Scientific Corporation - Location: Arden Hills US-MN, United States | N/A (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://bostonscientific.eightfold.ai/careers/job/563602812176386 - Excerpt: Design Assurance CAPA Manager - Cardiac Rhythm Management and Diagnostics (CRMDx) Arden Hills US-MN, United States | N/A ### Senior Therapeutic Specialist - Gilead Sciences - Location: Norway - Oslo (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Norway---Oslo/Senior-Therapeutic-Specialist_R0052304-1 - Excerpt: Senior Therapeutic Specialist Norway - Oslo posted: Posted 30 Days Ago ### Design Assurance CAPA Manager - Cardiac Rhythm Management and Diagnostics (CRMDx) - Boston Scientific - Location: Arden Hills, MN (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 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://jobs.bostonscientific.com/job/Arden-Hills-Design-Assurance-CAPA-Manager-Cardiac-Rhythm-Management-and-Diagnostics-%28CRMDx%29-MN-55112/1388419600/ - Excerpt: Design Assurance CAPA Manager - Cardiac Rhythm Management and Diagnostics (CRMDx) Arden Hills, MN Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. About This Role: This Manager of the Arden Hills based Cardiac Rhythm Management and Diagnostics (CRMDx) Field CAPA team will lead a team of 4-5 direct individuals and a number of cross functional teams to determine actionable root cause and implement effective solutions for high visibility issues impacting Active Implantables, Medical Electrical Equipment (MEE) & Accessories product performance within the CRMDx division. This role is a tremendous opportunity for a strong technical leader, with an innate technical curiosity, who is seeking leadership, complex problem-solving, project management experience, and making a direct impact on the lifesaving and life-enhancing technologies in CRMDx and Active Implantables. The role also provides great exposure to the intricacies of how the entire portfolio of CRMDx products function, are designed, and the many parts of the organization that support their commercial use. This individual will collaborate and partner with Research & Development, Regulatory, Market ### Senior Therapeutic Specialist II - Gilead Sciences - Location: China - Tianjin (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Tianjin/Senior-Therapeutic-Specialist-II_R0052081-1 - Excerpt: Senior Therapeutic Specialist II China - Tianjin posted: Posted 30+ Days Ago ### Veterinary Integration Lead – Therapeutic Diagnostics - Zoetis - Location: Parsippany (unspecified) - Salary: Not disclosed - Posted: 2026-05-21 - 401(k) match: listed (not source-backed) - Apply: https://zoetis.wd5.myworkdayjobs.com/zoetis/job/Parsippany/Veterinary-Integration-Lead---Therapeutic-Diagnostics_JR00020827-1 - Excerpt: Veterinary Integration Lead – Therapeutic Diagnostics Parsippany posted: Posted 22 Days Ago ### Sr Therapeutic Specialist - HIV - Gilead Sciences - Location: Australia - Sydney (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Australia---Sydney/Sr-Therapeutic-Specialist_R0051369-2 - Excerpt: Sr Therapeutic Specialist - HIV Australia - Sydney posted: Posted 30+ Days Ago ### Senior Therapeutic Area Specialist, Cardiovascular Community - Upper Manhattan E - Bristol Myers Squibb - Location: MANHATTAN - NY - US (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/MANHATTAN---NY---US/Senior-Therapeutic-Area-Specialist--Cardiovascular-Community---Upper-Manhattan-E_R1601467-2 - Excerpt: Senior Therapeutic Area Specialist, Cardiovascular Community - Upper Manhattan E MANHATTAN - NY - US posted: Posted 30+ Days Ago ### Sr Therapeutic Specialist (愛知県) - 肝臓領域 - Gilead Sciences - Location: Japan - Tokyo (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Japan---Tokyo/Sr-Therapeutic-Specialist------_R0052840-6 - Excerpt: Sr Therapeutic Specialist (愛知県) - 肝臓領域 Japan - Tokyo posted: Posted Today ### Senior Clinical Trial Associate - Olema Pharmaceuticals - Location: San Francisco, California (unspecified) - Salary: $110K-$120K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/olema/jobs/5842651004 - Excerpt: Senior Clinical Trial Associate San Francisco, California Olema Oncology is dedicated to developing better medicines for breast cancer and beyond. Our lead program, palazestrant (OP-1250), is a complete estrogen receptor antagonist (CERAN) currently in development for metastatic breast cancer with blockbuster potential as a monotherapy and in combination in ER+/HER2- metastatic breast cancer. Our follow-on product candidate, OP-3136, is a potent KAT6 inhibitor with best-in-class potential. Our scientific breakthroughs are accelerated through the ways in which we fearlessly support, motivate, and challenge one another. At Olema, we know that when we put people first, our work becomes second to none. If you're ready to join us at the edge of something unstoppable, let's make a profound impact together for our patients, for your career, for what's beyond . You can view our latest corporate deck and other presentations here . About the Role >>> Senior Clinical Trial Associate As the Senior Clinical Trial Associate reporting to the Senior Manager, Clinical Trial Leader, you will provide comprehensive administrative and operational support to clinical team members across all study activities, including both in-house and outsourced trials. This role supports cross-functional study execution through coordination with internal teams, external vendors, and site staff, and may include contributing to study documentation such as informed consent forms (ICFs) and central IRB submissions, supporting site payments and other study-related operational activities, as well as liaising with and following up with investigator sites. Responsibilities include assisting with study start-up, maintenance, and closeout activities; managing study documentation and ### Sr Therapeutic Specialist（関西） - Gilead Sciences - Location: Japan - Tokyo (unspecified) - Salary: Not disclosed - Posted: 2026-06-03 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Japan---Tokyo/Sr-Therapeutic-Specialist--_R0052782-4 - Excerpt: Sr Therapeutic Specialist（関西） Japan - Tokyo posted: Posted 9 Days Ago ### Senior Medical Director - Mineralys Therapeutics Inc - Location: US Remote (remote) - Salary: $330K-$364K - Posted: 2026-05-26 - Apply: https://job-boards.greenhouse.io/mineralystherapeutics/jobs/5231140008 - Excerpt: Senior Medical Director 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 Senior Medical Director will serve as a strategic and scientific leader responsible for shaping and executing the global medical affairs strategy in support of the company's pipeline and future commercial products. This physician leader will bridge Clinical Development and Commercial, ensuring scientific integrity, evidence generation, and external engagement across key stakeholders. This role will oversee Health Economics and Outcomes Research (HEOR) and Strategic Alliances & External Engagement and will play a critical role in preparing the organization for regulatory milestones and commercialization. Key Responsibilities Medical Strategy & Leadership - Develop and lead the global Medical Affairs strategy aligned with clinical development plans and commercial objectives - Serve as a key medical voice in cross-functional leadership discussions, including Clinical, Regulatory, Commercial, and Market Access - Translate clinical and scientific data into impactful medical strategies that support product differentiation and value demonstration Scientific Engagement & External Leadership - Build and maintain relationships with Key Opinion Leaders (KOLs), academic institutions, and clinical investigators - Represent the company at scientific congresses, ### Head, Oncology Immune Therapeutics - Novartis - Location: Cambridge (USA) (unspecified) - Salary: Not disclosed - Posted: 2026-05-21 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Cambridge-USA/Head--Oncology-Immune-Therapeutics_REQ-10078504 - Excerpt: Head, Oncology Immune Therapeutics Cambridge (USA) posted: Posted 22 Days Ago ### Finance Director - Synapticure - Location: United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-07 - Apply: https://jobs.lever.co/synapticure/fc60f420-6a00-416d-a700-4db3b7ab6fe8 - Excerpt: Finance Director United States About Synapticure Synapticure is the largest, most comprehensive specialty care clinic in the country for those living with neurodegenerative diseases. Founded by patients and caregivers living with these diseases, we are redefining the care journey for diseases like Alzheimer's, Parkinson's, and ALS in all 50 states. With a virtual care model, we democratize flexible, specialized care for patients and caregivers across the country. Our team creates personalized guided journeys focused on education and empowerment, while relentlessly working to facilitate access to clinical trials and expert multidisciplinary care providers like neurologists, psychologists, and care coordinators who collaborate to provide comprehensive patient care. To serve the millions of patients and caregivers living with neurodegenerative diseases, Synapticure requires determined, compassionate team members who are eager to engage patients who would benefit from Synapticure's care. About the Role As the Finance Director, you will serve as the strategic pillar for Synapticure's forward-looking financial runway. Reporting directly to the Chief Financial Officer (CFO), you will own enterprise-wide financial forecasting, corporate budgeting, and strategic modeling processes. This role requires a forward-thinking, highly strategic builder rather than a traditional financial reporter. You will act as a critical translator-synthesizing big, open-minded ideas from our growth team into robust financial frameworks, while integrating them seamlessly into our master model. You will work cross-functionally to evaluate new payer partnerships, care delivery models, and grant-funding streams. This is a high-impact role perfect for a finance leader who thrives in a fast-paced, early-stage environment. The Day to Da ### Senior Scientist, Multiomic Therapeutics - Johnson & Johnson - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-04 - 401(k) match: listed (not source-backed) - Apply: https://jj.wd5.myworkdayjobs.com/JJ/job/Madrid-Spain/Senior-Scientist--Multiomic-Therapeutics_R-059563 - Excerpt: Senior Scientist, Multiomic Therapeutics 2 Locations posted: Posted 8 Days Ago ### Senior Director, Medical Affairs Operations and Strategy - Definium Therapeutics - Location: Remote (remote) - Salary: $269K-$295K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5973783004 - Excerpt: Senior Director, Medical Affairs Operations and Strategy 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! Responsibilities: In collaboration with Medical Affairs leadership, develop, operationalize, and continuously refine the Medical Affairs strategy, helping to translate strategic objectives into actionable project plans, KPIs and timelines Oversee and ensure the quality of the departmental strategic planning processes, including operations tasks, and other activities related to pipeline compounds Leads organization, updating and communication of strategic plans to internal and external stakeholders ### Director, HEOR Strategy - Aesthetics - AbbVie Inc. - Location: South San Francisco, CA, 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/3743990013399946-director-heor-strategy-aesthetics - Excerpt: Director, HEOR Strategy - Aesthetics South San Francisco, CA, 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: AbbVie seeks a Director for the Aesthetics & Regenerative Medicine HEOR-Strategy team to lead strategic research for pipeline and on-market products, supporting approval, reimbursement, and differentiation. AbbVie has a robust Aesthetics & Regenerative Medicine portfolio with over 30 products in the pipeline, including both cash-pay and reimbursed drugs and devices. The role requires expertise in patient-centered outcomes research, HEOR strategy, and regulatory submissions, with responsibilities spanning both cash-pay and reimbursed portfolios. The Director may manage 1-2 direct reports. Responsibilities: Lead patient centered outcomes research (PCOR) and collaborate with the clinical development organization on co-primary and secondary PRO endpoints required for approval globally Lead PRO strategy, PRO development/implementation, and global regulatory submissions to enable approvals for drugs and devices Develop and execute HEOR strategic plans, including real-world evidence studies, economic modeling, and payer dossier to support product approval, market access, reimbursement, and differentiation Develop strategic plans and budgets in collaboration with cross-functional ### CV Therapeutic Area Lead - Amgen - Location: South Korea - Seoul (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://amgen.wd1.myworkdayjobs.com/Careers/job/South-Korea---Seoul/CV-Therapeutic-Area-Lead_R-234326-3 - Excerpt: CV Therapeutic Area Lead South Korea - Seoul posted: Posted 30+ Days Ago ### Senior Therapeutic Specialist, Oncology - Gilead Sciences - Location: 7 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/United-States---Field/Senior-Therapeutic-Specialist--Oncology_R0052354-1 - Excerpt: Senior Therapeutic Specialist, Oncology 7 Locations posted: Posted 30+ Days Ago ### Clinical Trial Manager or Associate Clinical Trial Manager - Rapport Therapeutics Inc - Location: 99 High Street, Suite 2100 , Boston, MA 02110 (unspecified) - Salary: $115K-$135K - Posted: 2026-04-23 - Apply: https://www.rapportrx.com/careers-board/?gh_jid=5041852007 - Excerpt: Clinical Trial Manager or Associate Clinical Trial Manager 99 High Street, Suite 2100 , Boston, MA 02110 When our people share why they joined Rapport and love it here, it comes down to three things: the science, the mission, and the team. At Rapport, we're driven by a passion for developing precision neuromedicines with the potential for fewer side effects, enabling patients and their families to enjoy healthier, more fulfilling lives. And we're doing this with extraordinary science and awesome people (affectionately called Rapptors). Our innovative scientific platform is centered on Receptor Associate Proteins (RAPs). RAPs are a component of neuronal receptor complexes, which play a crucial role in regulating receptor assembly and function. This precision approach has the potential to revolutionize the development of small molecule therapies. We are excited about the potential of our lead program, RAP-219. Our first indication targets focal epilepsy with additional clinical trials for neuropathic pain and bipolar disorder. The strength of Rapport comes from our Rapptors - who are united by our mission to improve patients lives. We bring the heart and hustle to advance our science forward, always staying true to our core values. We hope you're as excited about this opportunity as we are! This role is based in Boston, MA with onsite presence required Monday-Wednesday Your impact: In this role, you'll work with our Clinical Operations Leads to help keep trials running smoothly across multiple indications. It's a hands-on, high-impact role on a fun, driven team where you'll grow fast ### 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 ### Information Security Lead - Click Therapeutics - Location: New York, NY (unspecified) - Salary: $130K-$200K - Posted: 2026-02-25 - 401(k) match: listed (not source-backed) - Fertility benefits: yes (not source-backed) - Learning budget: yes (not source-backed) - Apply: https://job-boards.greenhouse.io/clicktherapeutics/jobs/8414783002 - Excerpt: Information Security Lead New York, NY Who We Are: Click Therapeutics, Inc., develops, validates, and commercializes software as prescription medical treatments for people with unmet medical needs. As a leading innovator of Digital Therapeutics™, Click delivers accessible, clinically proven, FDA-regulated prescription treatments to the smartphone in your hand. Click's treatments are defined by a commitment to applying technical and scientific rigor and patient-centric design to the development process. This results in uniquely engaging experiences that achieve compelling clinical outcomes for patients seeking new treatment options. Click Therapeutics continuously expands and refines its platform with novel cognitive, behavioral and neuromodulatory mechanisms of action and advanced data-driven tools such as artificial intelligence and machine learning. The digital therapeutics under development on Click's platform address diverse areas of therapeutic need, including indications in psychiatry, neurology, oncology, immunology, and cardiometabolic diseases. Consistently named a best place to work, Click fosters an inclusive, diverse workforce of innovators, clinicians, scientists, researchers, designers, technologists, engineers and more, united in a common mission to provide patients everywhere access to safe and effective prescription digital therapeutics. For more information, visit www.clicktherapeutics.com and connect with us on LinkedIn. About the Role: As Information Security Lead, you'll be at the forefront of safeguarding our groundbreaking digital therapeutics. We're seeking an individual with deep technical expertise in information security in the healthcare sector, ready to tackle complex challenges and pioneer innovative solutions. This isn't just a role; it's an opportunity to build, mentor, and inspire a high-performing team, while strategically collaborating across ### Principal Scientist, Peptide Therapeutics - Genentech, Inc. - Location: South San Francisco, California, United States of America (unspecified) - Salary: Not disclosed - Posted: 2026-02-24 - 401(k) match: listed (not source-backed) - Apply: https://roche.wd3.myworkdayjobs.com/ROG-A2O-GENE/job/South-San-Francisco/Principal-Scientist--Peptide-Therapeutics_202602-103654/apply - Excerpt: Principal Scientist, Peptide Therapeutics South San Francisco, California, United States of America This is a primarily lab-based, technical leadership position within the Peptide Therapeutics department. In this lab-based leadership role, you will combine hands-on synthetic expertise with strategic... ### Therapy Development Manager (Tampa, FL) - Pulse Biosciences Inc - Location: US Remote (remote) - Salary: Not disclosed - Posted: 2026-05-01 - Apply: https://job-boards.greenhouse.io/pulsebiosciences/jobs/5206792008 - Excerpt: Therapy Development Manager (Tampa, FL) US Remote Pulse Biosciences (Nasdaq: PLSE): Join the Future of Bioelectric Medicine Pulse Biosciences is a novel bioelectric medicine company committed to health innovation that has the potential to improve the quality of life for patients. The Company's proprietary CellFX® nsPFA™ (nanosecond Pulsed Field Ablation) technology delivers nanosecond pulses of electrical energy to non-thermally ablate cells while sparing adjacent noncellular tissue. The Company is actively pursuing the development of its CellFX nsPFA technology for use in the surgical treatment of atrial fibrillation and percutaneously in a select few other markets where it could have a profound positive impact on healthcare for both patients and providers. Visit pulsebiosciences.com to learn more. Why Join Us? At Pulse Biosciences, we are driven by purpose and innovation. - Our Mission: To build a viable Company that designs, produces, and commercializes nano-pulse technology to improve and extend the lives of patients. To solve the needs of patients, physicians, and healthcare providers with high quality and high reliability products and services, developed in accordance with rigorous scientific, engineering, and clinical standards. We exist to make a positive difference in the lives of patients, physicians, healthcare providers, shareholders and our Pulse Biosciences team members. - Our Culture: A community of creative, forward-thinking individuals tackling challenges with ingenuity and collaboration. - Our Commitment: Hiring the best and brightest minds to advance our world-class organization. What You Will Experience: - Culture and Purpose - Purposeful and rewarding work collaborating with bright and curious minds ### Sr. Therapeutic Specialist- RA（愛知） - Gilead Sciences - Location: Japan - Tokyo (unspecified) - Salary: Not disclosed - Posted: 2026-05-25 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/Japan---Tokyo/Sr-Therapeutic-Specialist--RA--_R0049919-1 - Excerpt: Sr. Therapeutic Specialist- RA（愛知） Japan - Tokyo posted: Posted 18 Days Ago ### Specialist, CAPA I - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013513176-specialist-capa-i - Excerpt: Specialist, CAPA I North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Performs root cause investigations for exceptions/nonconformities/deviations to required procedures and/or specifications for drug product manufacturing and packaging. Responsibilities Provides consistent and thorough exception documents and timely resolution of investigations based on CAPA requirements Coordinates the exception document process and creates exception documents Promotes culture of continuous improvement by identifying problems, conducting root cause analysis and confirming appropriate implementation of corrections, corrective and preventive actions Ensures all investigations are written according to corporate and site requirements Participates in implementation and maintenance of the Quality System to meet all applicable regulatory requirements Effectively collaborates/partners with other Quality areas and departments within the plant Qualifications: Bachelor's degree required. Preferably in one of the following areas: Biology, Chemistry or Engineering. 4+ years of experience in the pharmaceutical industry in Manufacturing, Quality or Engineering. Ability to problem solve and utilize analytical skills. Knowledge of Quality/Compliance management, Regulations and Standards. Additional Information: Applicable only to applicants applying to a position in any location with pay disclosure ### Therapeutic Specialist - Miami North - Insmed Incorporated - Location: Miami N, FL (unspecified) - Salary: Not disclosed - Posted: 2026-05-20 - Apply: https://insmed.wd5.myworkdayjobs.com/External/job/Miami-N-FL/Therapeutic-Specialist---Miami-North_R3479 - Excerpt: Therapeutic Specialist - Miami North Miami N, FL posted: Posted 23 Days Ago ### Regional Strategic Sales Director - Central - Heartflow INC - Location: Atlanta, GA; Nashville, TN; St. Louis, MO (unspecified) - Salary: Not disclosed - Posted: 2026-03-27 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/heartflowinc/jobs/5839650004 - Excerpt: Regional Strategic Sales Director - Central Atlanta, GA; Nashville, TN; St. Louis, MO Heartflow is a medical technology company advancing the diagnosis and management of coronary artery disease, the #1 cause of death worldwide, using cutting-edge technology. The flagship product-an AI-driven, non-invasive cardiac test supported by the ACC/AHA Chest Pain Guidelines called the Heartflow FFR CT Analysis-provides a color-coded, 3D model of a patient's coronary arteries indicating the impact blockages have on blood flow to the heart. Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMap™Analysis), assess coronary blood flow (FFR CT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis). Our pipeline of products is growing and so is our team; join us in helping to revolutionize precision heartcare. Heartflow is a publicly traded company (HTFL) that has received international recognition for exceptional strides in healthcare innovation, is supported by medical societies around the world, cleared for use in the US, UK, Europe, Japan and Canada, and has been used for more than 500,000 patients worldwide. The Regional Strategic Sales Director (RSD) is a high-impact leadership role responsible for the strategic expansion, and long-term adoption of Heartflow's portfolio.The RSD will focus on high-level C-suite engagement, CV service line optimization, and scaling Heartflow's full suite of solutions across the region. For FY26, the immediate priority is the successful launch of PCI Navigator - Heartflow's new pre-procedural planning solution for Percutaneous Coronary Intervention (PCI). Job Responsibilities: ### Associate Director Therapeutic Area Genetics (Immunology) - Regeneron Pharmaceuticals - Location: TARRYTOWN (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - 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://regeneron.wd1.myworkdayjobs.com/Careers/job/TARRYTOWN/Associate-Director-Therapeutic-Area-Genetics--Immunology-_R46254 - Excerpt: Associate Director Therapeutic Area Genetics (Immunology) TARRYTOWN posted: Posted 4 Days Ago ### Therapeutic Area Head, Oncology - Bristol Myers Squibb - Location: Uxbridge - GB (unspecified) - Salary: Not disclosed - Posted: 2026-05-26 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Uxbridge---GB/Therapeutic-Area-Head--Oncology_R1602621 - Excerpt: Therapeutic Area Head, Oncology Uxbridge - GB posted: Posted 17 Days Ago ### Corporate Counsel, Clinical Contracts - Summit Therapeutics - Location: Remote (US) (remote) - Salary: $158K-$185K - Posted: 2026-05-27 - Apply: https://job-boards.greenhouse.io/summittherapeutics/jobs/4259982009 - Excerpt: Corporate Counsel, Clinical Contracts Remote (US) About Summit: Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence. Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including: Non-small Cell Lung Cancer (NSCLC) - HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. - HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC. - HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC. Colorectal Cancer (CRC) - HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy. Ivonescimab is an ### Therapeutic Specialist, Hepatology - BC & Saskatchewan - GSK plc - Location: 5 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-19 - 401(k) match: listed (not source-backed) - Apply: https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/Canada--British-Columbia--Vancouver/Therapeutic-Specialist--Hepatology---BC---Saskatchewan_439650-1 - Excerpt: Therapeutic Specialist, Hepatology - BC & Saskatchewan 5 Locations posted: Posted 24 Days Ago ### Associate Director, Biostatistics - Definium Therapeutics - Location: Remote (remote) - Salary: $184K-$209K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/definiumtherapeutics/jobs/5848284004 - Excerpt: Associate Director, Biostatistics 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 an Associate Director, Biostatistics this person will provide statistical support for pipeline compounds' clinical development, regulatory filing, and commercialization. Reporting to Vice President, Head of Biometrics and Data Science, the successful candidate will serve as the biostatistician for assigned clinical trials to provide statistical leadership from trial design, data analysis, to results interpretation and dissemination. This role will also provide statistical support to regulatory filing ### Vice President, Drug Safety & Pharmacovigilance - Braveheart - Location: San Francisco, CA or Remote or Hybrid (hybrid) - Salary: $330K-$400K - Posted: 2026-05-20 - Apply: https://job-boards.greenhouse.io/braveheartbio/jobs/4254374009 - Excerpt: Vice President, Drug Safety & Pharmacovigilance San Francisco, CA or Remote or Hybrid About us: Braveheart Bio is a Bay Area-based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. Our lead program is a next-generation myosin inhibitor, licensed from Hengrui Pharma, being developed to transform the treatment of hypertrophic cardiomyopathy (HCM)-the most common inherited cardiac disease. Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our candidate has demonstrated a compelling clinical profile that may position it as a best-in-class therapy with meaningful differentiation. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a high-profile and rapidly evolving therapeutic area. The role: The Vice President, Drug Safety and Pharmacovigilance will lead and scale the global drug safety and pharmacovigilance function at Braveheart Bio. Reporting into the Chief Medical Officer, the VP is accountable for the safety strategy and integrated benefit-risk profile across the portfolio, with immediate focus on supporting Phase 3 programs and preparing the organization for NDA submission and post-marketing readiness. The VP will partner with an established Senior Director of PV (a direct report) to design the PV operating model, select CRO/PV vendor partners, establish the safety governance framework, and represent Safety in cross-functional and regulatory interactions. This individual will be hands-on while setting strategic direction and has a track record of leveraging external partners to deliver inspection-ready DSPV at ### Therapeutic Specialist, Salt Lake City - Insmed Incorporated - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - Apply: https://insmed.wd5.myworkdayjobs.com/External/job/NJ-Corporate-Headquarters/Therapeutic-Specialist--Salt-Lake-City_R3512 - Excerpt: Therapeutic Specialist, Salt Lake City 2 Locations posted: Posted 4 Days Ago ### 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 ### Director, Therapeutic Area Strategy, CRM - Novartis - Location: Basel (City) (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Basel-City/Director--CRM-Therapeutic-Area-Strategy_REQ-10076215-1 - Excerpt: Director, Therapeutic Area Strategy, CRM Basel (City) posted: Posted 30+ Days Ago ### Associate Director, Pipeline & Portfolio Market Planning - Corcept Therapeutics - Location: Redwood City, California, United States (unspecified) - Salary: $215K-$253K - Posted: 2026-04-27 - 401(k) match: listed (not source-backed) - Apply: https://www.corcept.com/careers/current-opportunities/?gh_jid=5982908004 - Excerpt: Associate Director, Pipeline & Portfolio Market Planning 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 Associate Director, Pipeline and Portfolio Market Planning is accountable for developing product strategies across Corcept's oncology portfolio. This individual will guide indication selection and sequencing, competitive landscape assessments, target product profiles (TPPs), product proposition, and long-range financial forecasting to inform program-level decision-making . Responsibilities: - Lead program-level strategy initiatives to define product vision, optimize lifecycle value, and drive business impact - Provide integrated physician, patient, and payer perspective in clinical strategy and new product planning initiatives - Own the design, implementation, and continuous refinement of competitive intelligence and market analysis frameworks that proactively inform program, investment, and governance decisions - Support cross-functional teams, including Commercial, Medical, Development, and Research, to ensure alignment and strategic continuity across the product lifecycle - Develop, maintain, and communicate long-range revenue forecasts and valuation models to support program planning ### Therapeutic Specialist, HCV/PBC -- Macon/Savannah - Gilead Sciences - Location: United States - Field (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/United-States---Field/Sr-Therapeutic-Specialist--HCV-PBC----Macon-Savannah_R0050403 - Excerpt: Therapeutic Specialist, HCV/PBC -- Macon/Savannah United States - Field posted: Posted 30+ 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. ### Therapeutic Specialist - Northern Houston - Insmed Incorporated - Location: North Houston, TX (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Apply: https://insmed.wd5.myworkdayjobs.com/External/job/North-Houston-TX/Therapeutic-Specialist---Northern-Houston_R3236 - Excerpt: Therapeutic Specialist - Northern Houston North Houston, TX posted: Posted 30+ Days Ago ### Director, Therapeutic Area Strategy, Immunology - Novartis - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Cambridge-USA/Director--Therapeutic-Area-Strategy--Immunology_REQ-10076236 - Excerpt: Director, Therapeutic Area Strategy, Immunology 2 Locations posted: Posted 30+ Days Ago ### Senior Clinical Trial Manager - Braveheart - Location: San Francisco, CA or Remote or Hybrid (hybrid) - Salary: $160K-$185K - Posted: 2026-05-05 - Apply: https://job-boards.greenhouse.io/braveheartbio/jobs/4240244009 - Excerpt: Senior Clinical Trial Manager San Francisco, CA or Remote or Hybrid About us: Braveheart Bio is a Bay Area-based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. Our lead program is a next-generation myosin inhibitor, licensed from Hengrui Pharma, being developed to transform the treatment of hypertrophic cardiomyopathy (HCM)-the most common inherited cardiac disease. Currently in Phase 3 clinical development in China for the more common obstructive form of HCM, our candidate has demonstrated a compelling clinical profile that may position it as a best-in-class therapy with meaningful differentiation. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a high-profile and rapidly evolving therapeutic area. The role: The Senior Clinical Trial Manager (Sr. CTM) is a key leader within the Clinical Operations team and will report to the Senior Director, Clinical Operations. The Sr. CTM will be responsible for the end-to-end operational delivery of a study in collaboration with other study leads across the program. This includes providing strategic oversight of study execution, vendor management, financial accountability, and cross-functional alignment. Key responsibilities: - Serve as the study lead for one or more global clinical trials, overseeing day-to-day execution from start-up through close-out (including site activation, enrollment, study conduct, and close-out) under the guidance of the Senior Director, Clinical Operations. - Partner closely with the Clinical Operations study leads on key decisions by providing recommendations, proactively identifying risks, and escalating ### Director, CVRM Genomics Therapeutic Area Lead - AstraZeneca - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - 401(k) match: listed (not source-backed) - Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/US---Boston---MA/Senior-Director--CVRM-Genomics-Therapeutic-Area-Lead_R-254044 - Excerpt: Director, CVRM Genomics Therapeutic Area Lead 2 Locations posted: Posted 4 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 ### Sr / Therapeutic Specialist - Oncology - Gilead Sciences - Location: China - Hong Kong (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/China---Hong-Kong/Sr---Therapeutic-Specialist---Oncology_R0051908-1 - Excerpt: Sr / Therapeutic Specialist - Oncology China - Hong Kong posted: Posted 30+ Days Ago ### Vice President, Senior Counsel – Commercial and Compliance - Mineralys Therapeutics Inc - Location: US Remote (remote) - Salary: $278K-$300K - Posted: 2026-04-14 - Apply: https://job-boards.greenhouse.io/mineralystherapeutics/jobs/5187831008 - Excerpt: Vice President, Senior Counsel – Commercial and Compliance 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. Vice President, Senior Counsel - Commercial & Compliance Mineralys is seeking an energetic, versatile, and highly driven attorney to serve as Senior Counsel, Commercial and Compliance. This individual will serve as a strategic legal partner to the Commercial and Medical Affairs teams and will report directly to the Chief Legal Officer. Prior experience assisting with commercial launch is essential. Key Responsibilities Commercial Legal Leadership - Serve as the primary legal advisor to the Commercial and Medical Affairs teams - Provide strategic counsel across pre-launch and launch activities, balancing legal risk with business objectives - Support commercialization readiness, including promotional strategy, market access, patient services, and distribution models - Draft, review, and negotiate a wide range of commercial agreements (e.g., vendors, patient support programs, speaker programs, distribution, market access) - Lead legal review of promotional and medical materials through MLR/PRC processes - Advise on interactions with HCPs, patients, payors, specialty pharmacies, and government entities - Support commercial and medical affairs activities, including speaker programs, advisory boards, ### Therapeutic Area Head, Psychiatry & Neuroscience Portfolio - Bristol Myers Squibb - Location: Uxbridge - GB (unspecified) - Salary: Not disclosed - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Uxbridge---GB/Therapeutic-Area-Head--Psychiatry---Neuroscience-Portfolio_R1603331 - Excerpt: Therapeutic Area Head, Psychiatry & Neuroscience Portfolio Uxbridge - GB posted: Posted Yesterday ### Director, Finance Specialty/Toxin - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (not source-backed) - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013517364-director-finance-specialty-toxin - Excerpt: Director, Finance Specialty/Toxin North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The primary objective of this position is to provide financial leadership, study forecasting, and business support for Specialty/Toxin therapeutic areas dynamic clinical portfolio within R&D Therapeutics, with portion of ~$2.5Bn spend. Specifically, this role partners closely with the therapeutic leadership teams to establish prioritization and align related programs across the respective therapeutic area and business partners to optimize available funding and ensure financial commitments are met, interacting with all levels of finance and business leadership. Core Responsibilities: Financial Planning and Analysis : Proactively lead the planning processes [Plan, LBE and LRP] ensuring accurate and timely integration of clinical study forecasts and other Externals spend types (PMed, CMC, etc.), ensuring senior management input to meet overall R&D / Corporate deadlines and deliverables. Ensure financial planning and reporting deliverables are accurate, clear and concise for Executive level review and approval. Ensure alignment of clinical assumptions with Commercial finance for Plan and LRP cycles. Sponsor and drive initiatives to significantly improve agility ### Team Lead, Therapeutic Area Quality - GSK plc - Location: 5 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/USA---Massachusetts---Boston/Team-Lead--Therapeutic-Area-Quality_442214 - Excerpt: Team Lead, Therapeutic Area Quality 5 Locations posted: Posted 7 Days Ago ### Director/Senior Director, Clinical Development (MD) - Axsome Therapeutics - Location: New York, NY (unspecified) - Salary: $240K-$300K - Posted: 2026-06-04 - Apply: https://job-boards.greenhouse.io/axsometherapeutics/jobs/5810241004 - Excerpt: Director/Senior Director, Clinical Development (MD) 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 a Director/Senior Director, Clinical Development to provide leadership across the full lifecycle of CNS programs, from IND through late-stage development and regulatory submission. The Director/Senior Director, Clinical Development will help shape clinical strategy, contribute to protocol design and key regulatory and clinical documents, and serve as a clinical representative with regulators, investigators, and cross-functional partners. This position will work closely with Clinical Operations, Regulatory, Biostatistics, Medical Affairs, HEOR, and Commercial teams, and will support high-quality study execution, data review, and program decision-making, while ensuring alignment with GCP and global regulatory standards. This role also contributes to regulatory interactions, publication planning, and ### Therapeutic Area Strategy Director, Oncology & Hematology - Novartis - Location: Basel (City) (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Basel-City/Therapeutic-Area-Strategy-Executive-Director--Oncology---Hematology_REQ-10074747 - Excerpt: Therapeutic Area Strategy Director, Oncology & Hematology Basel (City) posted: Posted 30+ Days Ago ### Senior Manager/Associate Director, Clinical FP&A - BridgeBio Pharma, Inc. - Location: San Francisco - 1800 Owens (unspecified) - Salary: $165K-$217K - Posted: 2026-02-24 - 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/5060274007 - Excerpt: Senior Manager/Associate Director, Clinical FP&A San Francisco - 1800 Owens 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. Who You Are Reporting to the Director of Clinical FP&A, the Senior Manager / Associate Director - Clinical FP&A will play a key role in supporting the governance and refinement of clinical trial expense management at BridgeBio. This individual will serve as an analytical resource and cross-functional partner, helping to contextualize clinical study expenses against operational performance metrics, identify and interpret drivers of financial variances, and build a stronger foundation for clinical financial analysis across our portfolio. Day-to-day, this person will ### Therapeutic Specialist - Hepatitis B/D - Minneapolis, MN - Gilead Sciences - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - 401(k) match: listed (not source-backed) - Apply: https://gilead.wd1.myworkdayjobs.com/gileadcareers/job/United-States---Field/Therapeutic-Specialist---Hepatitis-B-D---Minneapolis--MN_R0050306 - Excerpt: Therapeutic Specialist - Hepatitis B/D - Minneapolis, MN 2 Locations posted: Posted 30+ Days Ago ### 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 Therapeutic Area Specialist, Cardiovascular Community - Colorado N - Bristol Myers Squibb - Location: Denver - CO - US (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - 401(k) match: listed (not source-backed) - Apply: https://bristolmyerssquibb.wd5.myworkdayjobs.com/BMS/job/Denver---CO---US/Senior-Therapeutic-Area-Specialist--Cardiovascular-Community---Colorado-N_R1600746-1 - Excerpt: Senior Therapeutic Area Specialist, Cardiovascular Community - Colorado N Denver - CO - US posted: Posted 7 Days Ago ### Senior Director, Therapeutic Area - Piedmont Healthcare - Location: US, Blue Bell (ICON) (unspecified) - Salary: Not disclosed - Posted: 2026-05-14 - 401(k) match: listed (not source-backed) - Apply: https://icon.wd3.myworkdayjobs.com/broadbean_external/job/US-Blue-Bell-ICON/Senior-Director--Therapeutic-Area_JR146925-1 - Excerpt: Senior Director, Therapeutic Area US, Blue Bell (ICON) posted: Posted 29 Days Ago ### Senior Medical Director - Maze Therapeutics - Location: South San Francisco, CA (unspecified) - Salary: $338K-$412K - Posted: 2026-06-01 - 401(k) match: listed (not source-backed) - Mental health support: yes (not source-backed) - Apply: http://www.mazetx.com/careers/?gh_jid=8571653002 - Excerpt: Senior Medical Director South San Francisco, CA The Position At Maze Therapeutics, we are assembling a team of passionate, creative, and dedicated professionals to join us on our mission to turn groundbreaking genetic discoveries into life-saving medicines. We're looking for a Senior Medical Director to join our Clinical Sciences team and take a central role in pioneering the future of healthcare. As a Senior Medical Director, you'll be at the forefront of translating genetic insights into innovative treatments for patients . Your work will help drive the clinical development programs for game-changing therapies, starting with a small molecule that targets SLC6A19 - a novel therapeutic target for the treatment of chronic kidney disease and phenylketonuria . Maze Therapeutics has an exciting pipeline spanning both rare and common renal, cardiac, and metabolic diseases. In short, you'll play a fundamental part in advancing medical breakthroughs that have the potential to transform many lives. To succeed in this role, you'll need to thrive in a fast-paced, collaborative environment. As a Senior Medical Director for one or more development programs, you will partner closely with cross-functional team members and other technical experts to design, conduct, and interpret the key clinical studies, including first-in-human and proof-of-concept trials. Your contributions will be highly visible and integral to the success of the Maze team. This position reports to the Head of Clinical Development . The Impact You'll Have - Lead the design, execution, and analysis of clinical trials for the SLC6A19 program and other early-stage clinical assets ### Therapeutics Lead - Specialty - GSK plc - Location: Vietnam - Ho Chi Minh City (unspecified) - Salary: Not disclosed - Posted: 2026-05-15 - 401(k) match: listed (not source-backed) - Apply: https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/Vietnam---Ho-Chi-Minh-City/Therapeutics-Lead---Specialty_439022 - Excerpt: Therapeutics Lead - Specialty Vietnam - Ho Chi Minh City posted: Posted 28 Days Ago ### 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 ### Therapeutic Area Head – Respiratory - Apogee Therapeutics Inc - Location: Remote (remote) - Salary: $395K-$425K - Posted: 2026-06-11 - 401(k) match: listed (not source-backed) - Apply: https://job-boards.greenhouse.io/apogeetherapeutics/jobs/5160938007 - Excerpt: Therapeutic Area Head – Respiratory Remote About Apogee Therapeutics Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally. Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care. We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: C aring, O riginal, R esilient and E goless and a commitment to refusing to stop at “good enough”. If this sounds like you, keep reading! Role Summary We are seeking a Therapeutic Area (TA) Head, Respiratory - Clinical Development. In this --- Source-backed benefit claims include source links; other benefit values are labeled separately.