
10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
Biotechnology • Pharmaceuticals • Healthcare
Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.
🔥 39 minutes ago
🌐 United States, Canada – Remote
🌲 North Carolina – Remote
💵 $200k - $278.9k / year
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
👻 Ghost score 0%
Where this job comes from
Posted on Thermo Fisher Scientific's careers page, not through a job board
First seen by Remote Rocketship 39 minutes ago

10,000+ employees
🧬 Biotechnology
💊 Pharmaceuticals
🏥 Healthcare
Biotechnology • Pharmaceuticals • Healthcare
Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.
• Provide medical oversight of clinical trials to ensure company SOPs, client directives, good clinical practice, and regulatory requirements are followed • Manage and oversee contracted services throughout all stages of drug development • Attend and present at investigator and sponsor meetings • Provide medical consultation to clients, investigators, project teams, and associates • Support business development activities • Provide medical review and analysis of clinical trial serious adverse events • Ensure tasks delegated to medical monitors are properly executed • Provide therapeutic and protocol training • Write or review CSRs, IND/NDA reports, ICSRs, signal detection reports, periodic reports, RMPs, REMS, and CTD modules • Monitor safety variables, including adverse events, laboratory abnormalities, patient medical status, concomitant medications, and unblinding requests • Discuss medical concerns and clinical interpretations with principal investigators and clients • Review adverse events of special interest, serious adverse events, and clinical outcome events • Perform data review and validation, including coding listings and full safety data • Manage signal detection, review aggregate reports, contribute to label updates, and support dossier maintenance and risk management • Medically review adverse event and serious adverse event data from solicited, spontaneous, and literature sources
• MD or equivalent required • Formal training in Endocrinology Diabetes & Metabolism through residency and/or fellowship • Patient treatment experience comparable to 2 years • For Senior Medical Director: suitable clinical trial experience comparable to 1–2 years, or direct safety/Pharmacovigilance experience comparable to 2 years • Active medical licensure preferred but not required • Therapeutic expertise in Neurology • Strong decision-making, problem-solving, organizational, and analytical skills • Excellent oral and written communication skills • Working knowledge of relevant safety databases, such as MedDRA • Ability to travel domestically and internationally • Proficiency in basic computer applications • Fluent spoken and written English • Understanding of FDA, ICH, EMA, and GCP guidelines • Working knowledge of biostatistics, data management, and clinical operations procedures • Must be legally authorized to work in the United States or Canada without sponsorship • Must pass a comprehensive background check, including drug screening where applicable • Ability to work independently, prioritize sensitive complex information, mentor/train staff, and work under stress
• Annual incentive plan bonus • Healthcare • Employee benefits • Career and development prospects • Innovative, forward-thinking company culture
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