Website:
alzasyno.com
Job details:
Location: Gurugram, India
Company: AlzaSyno Life Sciences (CRO)
Role Overview
We are looking for a detail-oriented and proactive Pharmacovigilance Associate to support end-to-end drug safety activities, ensuring compliance with global pharmacovigilance standards.
Key Responsibilities:
• End-to-end ICSR processing (data entry, coding, assessment & narrative writing)
• Review and validation of adverse event reports
• MedDRA coding and safety data accuracy checks
• Case triage, seriousness & expectedness assessment
• Support aggregate reporting (PSUR, DSUR, PBRER)
• Literature screening & signal detection
• Maintain safety databases (Argus/ArisG or equivalent)
• Collaborate with cross-functional teams
• Support audits, inspections & quality checks
Who Can Apply?
• B.Pharm / M.Pharm / Pharm.D or Life Sciences graduates
• 0–3 years of Pharmacovigilance / Drug Safety experience
• Strong understanding of ICH-GCP & PV guidelines
• Familiarity with MedDRA & safety databases (Argus preferred)
• Strong analytical skills & attention to detail
Click on Apply to know more.