Senior Medical Safety Expert

2 weeks ago

tumakuru, India beBeeMedical Full time

Job OverviewThe primary objective of this position is to provide expert medical insights in the evaluation of safety data from various sources as part of the overall pharmacovigilance process.Conduct comprehensive medical reviews and clarify trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs)Develop, edit, and medically review Analyses of Similar Events (AOSE) for expedited casesProvide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications, or other medical data listingsThis role requires a deep understanding of Medicine, Pharmacovigilance- ICSR, and global, regional, and local clinical research regulatory requirements.The ideal candidate will possess excellent communication skills, both verbal and written, and be able to establish effective working relationships with managers, co-workers, investigative site staff, clients, and regulatory agency representatives.We are seeking an individual who can effectively work within a team environment and maintain accurate records of all project activities.This position offers opportunities for professional growth and development, with access to training programs and mentorship opportunities.

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