Infomerica, a leading staffing consultancy in the IT and healthcare domain, is actively hiring Drug Safety Associates with hands-on experience in Pharmacovigilance (PV), ICSR processing, and Argus Safety. This is an excellent opportunity for pharmacy graduates seeking career growth in drug safety and global pharmacovigilance operations.
Professionals with exposure to Individual Case Safety Reports (ICSR), MedDRA coding, causality assessment, and regulatory compliance are encouraged to apply.
This Drug Safety Associate job is ideal for candidates aiming to strengthen their pharmacovigilance expertise while working with structured SOP-driven global safety processes.
🔬 Key Responsibilities – Drug Safety Associate
As a Drug Safety Associate, you will be responsible for end-to-end ICSR processing and safety data management:
Case Processing & Validation
Receive adverse event reports from HCPs, patients, literature, and call centers
Validate cases based on minimum reporting criteria (identifiable patient, reporter, suspect drug, adverse event)
Perform data entry into safety databases (Argus, ARISg, Veeva Safety, etc.)
Conduct duplicate checks and ensure case completeness
Follow up for missing or incomplete safety information
Medical Review & Coding
Perform MedDRA coding for adverse events
Assess seriousness and expectedness of reported cases
Conduct causality assessments as per company SOPs
Ensure compliance with global regulatory timelines
Submit cases for medical review
This role requires strong knowledge of pharmacovigilance workflows, regulatory reporting standards, and safety database systems.
🎓 Qualifications & Eligibility
Bachelor of Pharmacy (B.Pharm) – Mandatory
1+ years of experience in Drug Safety / Pharmacovigilance
Hands-on experience in ICSR processing and Argus Safety
Strong understanding of MedDRA coding and global PV guidelines
Knowledge of regulatory timelines and case processing standards
Candidates with exposure to safety databases and global compliance frameworks will have a competitive advantage.
