Project Role: Associate Medical Safety Director
Work location: Pan India
Work Mode: Home Based
Must Have Skills: Signal Management and Aggregate Reporting.
Education: MBBS or MD is mandatory
Experience : 7+ of PV experience which includes 4+ years of signal and aggregate experience

Job Overview:

Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety’s involvement on assigned trials and standalone safety projects with appropriate oversight from management or more senior medical safety directors.

Essential Functions
Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary
Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements




Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported
Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a product’s safety profile
.Provide coding review of AEs, Past medical history, Concomitant medications, or other medical data listings to verify and medically vet clinical data
Represent safety and clinical data review findings during client meeting
Provide medical review and edits to IND Annual Reports, EU Periodic Perk Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Report
Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies
Provide medical oversight for label development, review, and change
Provide medical support and attendance at Data Safety Monitoring Board Meeting
Attends and contributes

📌 Associate Medical Safety Director Kochi
🏢 Iqvia
📍 Kochi