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1.0 - 5.0 years
0 - 0 Lacs
bangalore, chennai, united arab emirates
On-site
Roles and Responsibilities; Perform medical review of ICSRs for seriousness, causality, and expectedness. Assess adverse events (AEs/SAEs) in clinical trial and post-marketing settings. Write and validate concise and medically accurate narratives . Conduct literature review and assist in signal detection & risk analysis . Support preparation of aggregate reports (PSUR, DSUR, PBRER). Collaborate with PV scientists, data entry teams, and global medical reviewers. Qualifications: MBBS / BDS / BAMS / BHMS / Pharm.D / M.Pharm (Pharmacology) 1-5 years of experience in Pharmacovigilance, preferably in medical review/assessment roles Interested to apply can share you CV in Whatsapp/Call to 9342735755
Posted 3 days ago
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