Marketed Product Safety Specialist (QPPV, PVA) – IQVIA | Multiple Locations

IQVIA, a global leader in clinical research services, healthcare intelligence, and pharmacovigilance solutions, is inviting applications for the role of Marketed Product Safety Specialist. This is an excellent opportunity for life science professionals looking to build or strengthen their career in pharmacovigilance, lifecycle safety, and safety agreements management.

The position is open across multiple Indian locations, including Mumbai, Thane, Noida, and Chennai, offering exposure to global safety operations within a reputed CRO environment.

🔍 Job Summary

• Job Title: Marketed Product Safety Specialist I
• Job ID: R1522371
• Employment Type: Full-time
• Company: IQVIA
• Locations: Thane, Mumbai, Noida, Chennai (and other locations)
• Application Deadline: 22 January 2026
• Experience Level: Entry-level / Early career

🧩 Key Responsibilities (Pharmacovigilance Jobs at IQVIA)

• Assist in the development and preparation of pharmacovigilance safety agreements under direct supervision
• Collaborate with project teams to determine appropriate terms and conditions for safety agreements
• Prepare and update PSMF (Pharmacovigilance System Master File) documents for small to mid-size companies
• Act as a secondary customer interface on small projects
• Support preparation, review, finalization, and distribution of safety agreements
• Maintain and update safety agreement databases and documentation
• Provide operational support across assigned pharmacovigilance projects

🎓 Required Qualifications

• Associate’s Degree in Life Sciences, Business Management, or a related discipline
• Equivalent combination of education, training, or experience is acceptable
• Basic to good understanding of Lifecycle Safety and Pharmacovigilance processes
• Strong attention to detail and documentation accuracy
• Excellent written and verbal communication skills
• Ability to manage multiple projects simultaneously
• Strong organizational and time-management skills
• Proven ability to work collaboratively with internal teams and clients

💼 Why Join IQVIA?

• Work with a global leader in pharmacovigilance and clinical research
• Exposure to international safety agreements and compliance frameworks
• Structured learning under supervision—ideal for early-career professionals
• Career growth in drug safety, regulatory compliance, and lifecycle management
• Inclusive, collaborative, and knowledge-driven work culture

📩 How to Apply

Application Link