IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a focus on healthcare intelligence, IQVIA helps biotech, pharmaceutical, and medical device companies improve patient outcomes through data-driven insights.
📍 Location: Kolkata, India
💼 Job Type: Full-time, Office-based
Job Description: Safety Associate
As a Safety Associate at IQVIA, you will play a crucial role in pharmacovigilance (PV) case processing, ensuring compliance with global safety regulations.
Key Responsibilities:
✔ Process and manage adverse event (AE) reports in compliance with regulatory requirements.
✔ Utilize Argus safety database for case processing, data entry, and quality checks.
✔ Perform medical coding (MedDRA/WHO Drug) and narrative writing.
✔ Ensure timely and accurate submission of safety reports to regulatory authorities.
✔ Collaborate with global PV teams to maintain high-quality safety data.
Eligibility Criteria
✅ Education: B.Pharm / M.Pharm / Pharm.D
✅ Experience: 6 months – 1.5 years in PV case processing
✅ Mandatory Skills: Hands-on experience with Argus database
✅ Work Mode: Office-based (Kolkata)
Why Join IQVIA?
🔹 Global Exposure: Work with a top-tier life sciences company.
🔹 Career Growth: Opportunities in pharmacovigilance & drug safety.
🔹 Learning & Development: Training on global safety databases.
🔹 Competitive Salary & Benefits: Health insurance, paid leaves, and more.
How to Apply?
📩 Send your resume to: dhanalakshmy.tv@iqvia.com
📌 Subject Line: “Application for Safety Associate – Kolkata”
