Are you a pharmacovigilance professional looking to advance your career with a global leader in healthcare intelligence? IQVIA is hiring for the Safety Associate role in an office-based setting. If you have 1-2 years of experience in PV case processing and expertise in Argus Database, this could be your next big opportunity!
Job Details
- Position: pharmacovigilance Safety Associate
- Experience Required: 1-2 years in Pharmacovigilance (PV) Case Processing
- Mandatory Skills: Argus Database proficiency
- Educational Qualification: B.Pharm / M.Pharm / Pharm.D
- Mode of Work: Office-Based
Job Description
As a Safety Associate at IQVIA, you will play a crucial role in ensuring drug safety and compliance with global pharmacovigilance regulations. Your responsibilities will include:
✅ Case Processing: Handling Individual Case Safety Reports (ICSRs) from various sources.
✅ Argus Database Management: Entering, reviewing, and validating safety data in the Argus safety database.
✅ Regulatory Compliance: Ensuring adherence to global PV guidelines (FDA, EMA, etc.).
✅ Quality Checks: Performing data consistency checks and supporting audits.
✅ Collaboration: Working with cross-functional teams for safety data reconciliation.
Why Join IQVIA?
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With a focus on improving patient outcomes, IQVIA empowers professionals to drive innovation in healthcare.
🔹 Global Impact: Work on projects that shape the future of medicine.
🔹 Career Growth: Access to continuous learning and development programs.
🔹 Innovative Culture: Be part of a team that leverages AI and real-world data for healthcare advancements.
How to Apply?
If you meet the eligibility criteria and are excited about this opportunity, send your updated resume to:
📧 Email: dhanalakshmy.tv@iqvia.com
