The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department
Job Summary
The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials.
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale.
Matching Summary
The (Associate) Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the Pharmacovigilance department.
Skills & Requirements
Must-have
Medical leadership to study teams
Real-time medical monitoring
Medical point of contact for stakeholders
Ensure study compliance for medical aspects
Strong communication & presentation skills
Nice-to-have
Delivering life-changing therapies
Accelerate research and solve challenges
Valued diverse experiences and perspectives
Key Requirements
MD, MB/BS or equivalent degree
Strong medical knowledge
Clinical experience running Neurology patients
Significant experience within pharmaceutical industry
Experience with clinical trials
Experience with pharmaceutical medicine
Understanding of NDA submission process
Understanding of regulatory guidelines for adverse event reporting