Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
Medical Director – Rheumatology
Job not on LinkedIn
🕒 2 days ago
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Thermo Fisher Scientific
10,000+ employees
Founded 1956
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
Biotechnology • Pharmaceuticals • Science
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.
📋 Description
• Provides medical oversight of clinical trials to ensure compliance with SOPs, client directives, and regulations • Attends and presents at investigator and sponsor meetings • Provides medical consultation to clients, investigators, and project team members • Provides medical review and analysis for clinical trial serious adverse events and client deliverables • Ensures tasks delegated to PV are properly executed and adhere to applicable regulations • Monitors all safety variables of clinical studies • Discusses medical concerns with principal investigators and clients • Manages signal detection activities and contributes to label updates
🎯 Requirements
• MD or equivalent required • Active medical licensure preferred • Clinical experience in treating patients in the specialty or sub-specialty (comparable to 2 years) • Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2 years) • Direct experience in safety/Pharmacovigilance (comparable to 2 years) • Strong decision-making, problem solving, organizational skills and analytical skills • Excellent oral and written communication skills • Working knowledge of relevant safety databases (e.g. Medra) • Flexibility to travel domestically and internationally • Proficiency in basic computer applications • Fluent in spoken and written English • Ability to act as a mentor/trainer to other staff within PV
🏖️ Benefits
• Health insurance • Retirement plans • Paid time off • Flexible working arrangements • Professional development • Wellness programs
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