
10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
🔥 2 minutes ago
🌐 Mexico, Brazil, +4 more countries – Remote
⏰ Full Time
🟠 Senior
👨⚕️ Medical Director
👻 Ghost score 10%
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10,000+ employees
Founded 1956
🏥 Healthcare
📦 Logistics
🏭 Manufacturing
Healthcare • Logistics • Manufacturing
Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
• Provide medical oversight of psychiatric clinical trials • Ensure company SOPs, client directives, good clinical practice and regulatory requirements are followed • Manage and oversee contracted services throughout clinical trial development • Attend and present at investigator and sponsor meetings • Provide medical consultation to clients, investigators and project team members • Support business development activities • Provide medical review and analysis for clinical trial serious adverse events • Ensure tasks delegated to medical monitors are properly executed • Provide medical, therapeutic and protocol training • Monitor safety variables including adverse events, laboratory abnormalities, patient medical status, concomitant medications and un-blinding requests • Discuss medical concerns with principal investigators and clients and apply medical judgment to clinical situations • Review adverse events of special interest, serious adverse events and clinical outcomes events • Review coding listings and/or full safety data to assess potential safety concerns • Mentor and train other staff
• MD or equivalent required • Clinical experience in Psychiatry and formal training in Psychiatry (residency and/or fellowship) • Patient treatment experience comparable to 2 years • For Senior Medical Director: suitable clinical trial experience in a Contract Research Organization or pharmaceutical company comparable to 1–2 years • Preference toward clinical development/medical monitoring experience • Must be legally authorized to work in the hiring country without sponsorship • Must be able to pass a comprehensive background check, including drug screening where applicable • Therapeutic expertise in Psychiatry • Working knowledge of relevant safety databases, such as MedDRA • Fluent in spoken and written English • Understanding of FDA, ICH, EMA and GCP guidelines • Working knowledge of biostatistics, data management and clinical operations procedures • Proficiency in basic computer applications • Ability to travel domestically and internationally • Active medical licensure preferred but not required
• Annual incentive plan bonus • Healthcare • Employee benefits • Career and development prospects • Innovative, forward-thinking company culture • Collaboration and development opportunities
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