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IQVIA Hiring For Pharmacovigilance Team (Entry To Senior Level)

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challenging projects

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Are you looking for a career in Pharmacovigilance (PV) and Drug Safety? IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for four key roles in Bengaluru, Karnataka. If you have a background in life sciences, pharmacy, or medicine, this is a great opportunity to join a dynamic team in safety operations and pharmacovigilance.

📍 Location: Bangalore, India (Office-based)
📅 Job Type: Full-Time
⏳ Urgent Hiring – Apply Soon!


🔍 Detailed Job Descriptions

1. Operations Specialist 1 – Pharmacovigilance

Key Responsibilities:

  • Process safety data (adverse events, product complaints) as per SOPs, ICH-GCP, and regulatory guidelines.
  • Perform case processing, data entry, coding (MedDRA/WHO-DD), and narrative writing.
  • Ensure compliance with global pharmacovigilance regulations (FDA, EMA, etc.).
  • Work on safety databases and support medical review activities.

Qualifications:

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  • Bachelor’s degree in Life Sciences, Pharmacy, or related field.
  • 1-3 years of pharmacovigilance experience (freshers with relevant education may apply).
  • Strong knowledge of medical terminology and safety databases.

2. Safety Associate – Entry-Level PV Role

Key Responsibilities:

  • Assist in case processing, data entry, and tracking adverse events (AEs).
  • Support coding (MedDRA/WHO-DD) and document management.
  • Ensure compliance with SOPs and regulatory timelines.

Qualifications:

  • B.Pharm / M.Pharm / B.Sc / M.Sc in Life Sciences.
  • 0-1.5 years of experience (freshers eligible).
  • Basic knowledge of pharmacovigilance and medical terms.

3. Associate Manager, Safety Operations Team (Leadership Role)

Key Responsibilities:

  • Manage a team of safety specialists, ensuring compliance and productivity.
  • Oversee hiring, training, and performance reviews.
  • Lead process improvements and client communications.
  • Ensure timely regulatory submissions (FDA, EMA, etc.).

Qualifications:

  • Bachelor’s/Master’s in Life Sciences or Medicine.
  • 4-6 years of PV experience + 2 years in team management.
  • Strong leadership and SOP compliance skills.

🏆 Why Join IQVIA?

  • Global leader in clinical research and pharmacovigilance.
  • Career growth in drug safety and regulatory compliance.
  • Training & certifications in pharmacovigilance.
  • Hybrid/office-based roles in Bangalore.

📩 How to Apply?

Just Click On Below Text For Apply

1️⃣ Safety associate

2️⃣ Operations Specialist 1

4️⃣ Assoc Mgr, Safety Opns Team