Drug Development

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 ↗

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.

Listed on Merck’s careers site · Apply there ↗

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 ↗

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 ↗

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.

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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.

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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.

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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 ↗

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.

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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 ↗