Pharmacovigilance Scientist
2 weeks ago
**A leading contract research organization trusted by leaders**:
Position Code: PVS001
**Location**: Chandigarh
Manage activities relating to the processing, follow-up, analysis, and regulatory reporting of adverse events (AEs) and serious adverse events (SAEs) for marketed and investigational human and veterinary products in accordance with the applicable regulatory requirements. Aggregate report preparation [e.g. Periodic Benefit Risk Evaluation Reports (PBRERs)/ Periodic Safety Update Reports (PSURs), Addendum to Clinical Overviews (ACOs), Addendum PSURs, PSUR Line Listings, US Periodic Adverse Drug Experience Reports (PADERs)] from aggregate data for products, in accordance with client conventions and requirements; Quality checks of aggregate reports; Signal detection-related analyses and reports including cumulative analyses, issue event analyses.
**Minimum qualification**(s):
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