About the Role
As a Junior Drug Safety Associate, you will support end-to-end pharmacovigilance operations, ensuring accurate and compliant processing of Individual Case Safety Reports (ICSRs). This role is ideal for professionals with hands-on safety database experience looking to grow in a global PV environment.
Key Responsibilities:
Perform case intake, triage, and data entry of ICSRs (spontaneous, clinical trial, literature)
Conduct quality checks (QC) on safety cases
Ensure timely processing as per regulatory timelines
Maintain compliance with SOPs, ICH-GCP, and global PV regulations
Support periodic safety activities under senior guidance
Requirements
2–5 years of experience in Drug Safety / Pharmacovigilance
Hands-on experience with safety databases (Argus, ARISg, Safety Easy, or similar)
Knowledge of MedDRA and WHO-DD coding
Strong attention to detail and documentation skills
Life Sciences / Pharmacy / Medical background preferred