19 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
Associate Clinical Country and Site Lead (West Coast/Midwest)
Biogen
Remote, USA · $116,000 – $155,000
This role bridges local clinical trial operations and global development strategy for Biogen, requiring someone with substantial site management experience to coordinate between investigators, internal teams, and external partners across the West Coast or Midwest. It suits an experienced clinical research professional who can synthesize local market knowledge, drive site performance, and escalate complex issues while maintaining cross-functional relationships.
Listed on Biogen’s careers site · Apply there ↗
R&D Study Operation Oncology CRA
Merck
Full-time
This role oversees clinical trial operations for oncology drug development, managing investigator sites, recruitment, safety monitoring, and regulatory documentation. It suits experienced clinical research associates with oncology background who can coordinate between medical teams and company stakeholders.
Microsoft WordPowerPointClinical Data ManagementDrug DevelopmentMicrosoft ExcelRegulatory Compliance
Listed on Merck’s careers site · Apply there ↗
Director, Medical Safety Assessment Physician
Bristol Myers Squibb
Full-time · $255,860 – $310,040
Lead medical safety strategy and oversight for assigned pharmaceutical compounds across development and postmarketing phases, managing benefit-risk evaluations and regulatory submissions. Suited for physicians with pharmacovigilance experience who want to direct patient safety strategy at a major pharmaceutical company.
Listed on Bristol Myers Squibb’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 ↗
Executive Director, Clinical Development (MD), Inflammation and Immunology
Gilead Sciences
Full-time · United States - California - Foster City · $349,010 – $451,660
This role leads clinical development strategy and execution for inflammation and immunology programs at Gilead, managing complex multi-indication portfolios from early phase through Phase 3 trials. It suits experienced physician-scientists with strong regulatory and drug development backgrounds who can lead cross-functional teams and represent programs to health authorities.
Listed on Gilead Sciences’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 ↗
Sr Manager, Corporate Development
Gilead Sciences
Full-time · United States - California - Foster City · $169,320 – $219,120
This role leads strategic partnerships, investments, and acquisitions for Gilead's oncology, virology, and inflammation programs, collaborating across research, clinical, and commercial functions. It suits experienced professionals from biotech, pharma, consulting, or finance who understand drug development and can manage complex negotiations and cross-functional initiatives.
Listed on Gilead Sciences’s careers site · Apply there ↗
Principal Scientist, Regulatory Liaison
Merck
Full-time · $173,200 – $272,600
This role leads global regulatory strategy for vaccine and infectious disease products, serving as the primary regulatory contact between the company, FDA, and international agencies throughout drug development and commercialization. It suits experienced scientists with strong command of pharmaceutical regulation and the ability to work independently on complex, multi-indication programs.
Listed on Merck’s careers site · Apply there ↗
Director, Medical Safety Assessment Physician, 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 Principal Scientist, Clinical Research, Breast Cancer
Merck
Full-time · Rahway, NJ · $282,200 – $444,200
A senior oncology research leader will oversee the full lifecycle of breast cancer clinical trials and drug development programs, from early-stage design through post-market studies. This role suits experienced physicians or PhDs with substantial industry background who can manage complex research portfolios, work across cross-functional teams, and maintain deep scientific expertise in oncology.
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 ↗
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 ↗
Associate Director, Global Scientific and Regulatory Documentation, Content Strategy
Bristol Myers Squibb
Full-time · Princeton, NJ · $170,880 – $207,061
This role involves authoring and coordinating complex regulatory documents for clinical drug submissions across immunology and cardiovascular programs, ensuring compliance with global regulatory standards and internal documentation practices. The position suits experienced pharmaceutical professionals with strong scientific writing skills who can lead cross-functional teams and manage documentation strategy from early development through marketing authorization.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Senior Director, Clinical Research, Atherosclerosis
Merck
Full-time · $173,200 – $272,600
This role leads clinical research strategy and execution for atherosclerosis drugs across all development phases, from early-stage planning through post-market studies. It suits physicians or PhDs with substantial industry drug development experience who want to direct large clinical programs and work across cross-functional teams.
Listed on Merck’s careers site · Apply there ↗
Executive Director, Clinical Science, Ophthalmology & Neuroscience
Merck
$255,800 – $402,700
This senior leadership role oversees clinical science strategy and operations for ophthalmology and neuroscience drug development programs, directing a large team and ensuring scientific rigor while driving modernization through AI and digital capabilities. The position suits experienced pharmaceutical leaders with deep clinical development expertise who can balance portfolio delivery, organizational excellence, and talent development across a complex, matrixed environment.
Executive Director (Distinguished Scientist), Clinical Research, Atherosclerosis
Merck
Full-time · Rahway, NJ · $310,900 – $489,400
This role leads clinical development strategy and execution for atherosclerosis medicines from Phase 2 through regulatory submission, managing cross-functional teams and external research collaborations. It suits physicians with 5+ years of drug development experience who want to guide late-stage trials and regulatory interactions while maintaining active engagement with scientific literature and key opinion leaders.
Listed on Merck’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 ↗