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 – Cardiology
Job not on LinkedIn
🕒 May 12
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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
• Manage all medical aspects of contracted tasks across the pharmaceutical product life-cycle • Provide medical consultation to team members and answer all study-related medical questions • Provide therapeutic training and protocol training on assigned studies, as requested • Assist in writing (interpretation of safety and efficacy data) and/or reviewing CSR, IND/NDA reports, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc., to ensure that the medical content is accurate and complete • Monitor all safety variables (AE, laboratory abnormalities, changes in patient medical status) • Discuss all medical concerns with principal investigators and clients • Provide medical review of adverse events of special interest, serious adverse events, and clinical outcomes events reported by study sites
🎯 Requirements
• MD or equivalent required • Clinical experience in treating patients in the specialty or sub-specialty associated with the applicants training (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) in the industry • Direct experience in safety/Pharmacovigilance (comparable to 2 years) • Knowledge of relevant safety databases (e.g. Medra) • Fluent in spoken and written English
🏖️ Benefits
• Flexible work arrangements • Professional development opportunities
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