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)
Builds
Clinical trial safety data, regulatory submissions, and medical protocols for global clients.
Domain
Life Sciences / Clinical Research / Pharmacovigilance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Medical judgment and interpretation, safety signal identification, medical review of adverse event reports, protocol and report writing, therapeutic training, business development presentation
Preferred skills
Experience with pre and post approval services, connecting with medical communities
Technologies
None stated
Responsibilities
Lead medical aspects of contracted tasks and supervise safety variables; Analyze safety data to identify emerging signals; Review individual case safety reports and clinical outcome reports; Consult with clients, investigators, and healthcare professionals on medical issues; Assist in business development activities and present safety processes to clients; Train project teams on therapeutic and protocol matters; Write, review, and approve regulatory submissions and protocols.
Seniority
Senior, hands-on IC
