Senior Medical Director
Core
Provide medical support, advice, and monitoring for clinical trials and safety evaluation within the Pharmacovigilance department.
Role type
Senior Medical Director (Pharmacovigilance/Clinical Trials)
Builds
Medical safety processes, regulatory submissions, and clinical trial protocols for clients in the healthcare/pharma industry.
Domain
Life Sciences / Pharmacovigilance / Clinical Research
Required skills
Medical judgment, safety data analysis, regulatory submission writing, protocol development, therapeutic knowledge, business development, team training, report review.
Preferred skills
Experience in neuroscience, contract task leadership, emerging safety signal identification.
Technologies
Clinical trial management systems, safety reporting databases, regulatory submission platforms.
Responsibilities
Lead medical aspects of contracted tasks and supervise safety variables; consult with clients and investigators on medical issues; analyze safety data to identify emerging signals; review individual case safety reports and adverse event reports; assist in business development and present safety processes to clients; train project teams on protocols and therapeutics; write and approve reports and regulatory submissions.
Seniority
Senior, hands-on IC with leadership responsibilities.