12 open listings
Roles posted by organizations here, alongside roles we found on employers’ own careers sites. Crawled roles say so on the card and send you to the employer to apply. Only show organizations on Career App
MP
Corporate Development Lead, Life Sciences
Menlo Ventures Portfolio
Full-time · San Francisco, CA · $325,000 – $425,000
Anthropic is hiring a strategic leader to identify and execute deals in AI-applied life sciences—acquisitions, investments, and partnerships with biotech and clinical companies. The role suits someone with deep domain expertise in drug development, deal-making experience, and genuine technical fluency in AI.
Listed on Menlo Ventures Portfolio’s careers site · Apply there ↗
Director, WW Autoimmune Cell Therapy Medical Affairs
Bristol Myers Squibb
Full-time · Princeton, NJ · $207,490 – $251,433
This role leads medical affairs strategy for early-stage CAR T cell therapy programs targeting autoimmune diseases, requiring deep expertise in clinical development and the ability to coordinate across multiple departments to advance regulatory and commercial milestones. The position suits experienced medical affairs leaders or clinicians with strong cross-functional collaboration skills and a track record in cell therapy or complex therapeutic development.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Senior Director, Clinical Development Metabolism (MASH)
Merck
Full-time · $282,200 – $444,200
This role leads clinical development strategy and execution for new and existing drugs targeting metabolic liver disease and obesity-related disorders, particularly MASH. It suits senior physicians with extensive industry drug development experience and expertise in metabolic, endocrine, or hepatic medicine who want to shape late-stage trials and regulatory pathways.
Listed on Merck’s careers site · Apply there ↗
Director, Clinical Sciences, Oncology
Moderna
Full-time · $183,800 – $330,300
This role leads clinical development strategy and execution for oncology studies at a biotechnology company, overseeing data quality, regulatory compliance, and study operations from early to late phases. It suits experienced clinical scientists with advanced degrees and deep oncology expertise who can drive complex programs across multiple internal and external stakeholders.
Listed on Moderna’s careers site · Apply there ↗
Sr. Principal Scientist (Sr. Director) - Regulatory Liaison
Merck
Full-time · $190,800 – $300,300
A senior regulatory leadership role managing global approval strategies for cardiovascular and metabolic drugs from development through market launch. This suits experienced regulatory scientists who have led complex submissions with multiple indications and want to shape product strategy while working directly with FDA and international health authorities.
Listed on Merck’s careers site · Apply there ↗
Senior Director, Global Regulatory Lead Neuroscience
Bristol Myers Squibb
Full-time · $226,750 – $313,460
A senior regulatory leadership role at a major pharmaceutical company guiding the development and commercialization of neuroscience drugs globally. This position suits experienced regulatory professionals with scientific backgrounds who can navigate complex drug development, interface with health authorities, and lead strategic initiatives across multiple markets.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Senior Director, Oncology Clinical Development, Early Phase
Moderna
$210,900 – $379,200
Lead oncology clinical development strategy and execution for mRNA-based immunotherapies at an early-phase stage, working across cross-functional teams to design studies, develop regulatory submissions, and bring precision medicines to patients. This role suits experienced medical oncologists or hematologists with proven leadership in biopharmaceutical drug development who thrive in fast-paced environments.
Listed on Moderna’s careers site · Apply there ↗
Senior Director, Discovery Biology - Oncology Small Molecule
Merck
Full-time · Boston, MA · $194,100 – $305,600
This role leads the discovery and development of small molecule cancer drugs for a major pharmaceutical company, overseeing the progression from laboratory research through clinical testing. It suits experienced oncology scientists with a track record of bringing multiple drug candidates into human trials and the ability to mentor and guide senior research teams.
Listed on Merck’s careers site · Apply there ↗
Senior Director, Medical Safety Assessment Program Lead, Neuroscience
Bristol Myers Squibb
Full-time · $255,860 – $347,244
A Director-level physician role overseeing medical safety strategy and risk management for Bristol Myers Squibb's neuroscience compounds throughout development and post-market phases. This position suits experienced medical doctors with pharmacovigilance or clinical research backgrounds who can lead cross-functional safety teams and interact with regulators.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Senior Clinical Director, Clinical Research, Hematology
Merck
Full-time · $282,200 – $444,200
This role leads clinical research strategy and execution for blood cancer medicines across all development phases, from early-stage work through post-market studies. It suits experienced physician-scientists who want to shape drug development strategy and collaborate across functional teams in a large pharmaceutical environment.
Listed on Merck’s careers site · Apply there ↗
Director, Statistical Programming
Bristol Myers Squibb
Full-time · $216,570 – $293,921
A leadership role overseeing statistical programming delivery for a pharmaceutical therapeutic area, requiring both technical expertise in clinical trial programming and people management experience. This is for someone with 10+ years in pharma who can drive process improvement, mentor teams, and partner with senior stakeholders to execute complex drug development programs.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Distinguished Scientist, Clinical Research, Thoracic Malignancies
Merck
Full-time · $310,900 – $489,400
This senior pharmaceutical leadership role oversees the full lifecycle of clinical trials for thoracic cancer drugs, from early development through regulatory approval and publication. It suits an MD or MD/PhD with deep oncology expertise who has managed drug development in industry and can lead cross-functional teams while maintaining current scientific knowledge in their field.
Listed on Merck’s careers site · Apply there ↗