Pharmacovigilance Associate & Senior Pharmacovigilance Associate
Global CRO leader ICON Plc is hiring Pharmacovigilance Associates and Senior Pharmacovigilance Associates in Chennai and Trivandrum. This opportunity is ideal for professionals with experience in ICSR processing, adverse event reporting, MedDRA coding, WHO-DD coding, and drug safety operations.
📋 Job Overview
| Particulars | Details |
|---|---|
| Position | Pharmacovigilance Associate / Senior Associate |
| Company | ICON Plc |
| Location | Chennai & Trivandrum |
| Experience | 2–4 Years |
| Industry | Pharmacovigilance & Drug Safety |
| Employment Type | Full-Time |
💼 Key Responsibilities
- Collect, assess, and process adverse event reports.
- Perform ICSR processing and case management activities.
- Manage safety inbox and case intake activities.
- Perform case triage and database book-in.
- Prepare medical narratives and case documentation.
- Code events using MedDRA and WHO-DD.
- Conduct quality review and case validation.
- Support follow-up activities and reconciliation.
- Process literature-based ICSRs.
- Ensure compliance with PV regulations and SOPs.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Biochemistry
- Microbiology
- Nursing
- Healthcare Graduates
- Minimum 2 Years Pharmacovigilance Experience
⭐ Required Skills
- ICSR Processing
- Adverse Event Reporting
- Drug Safety Operations
- MedDRA Coding
- WHO-DD Coding
- Case Processing
- Pharmacovigilance Compliance
- Quality Review & Validation
- Clinical Trial Safety
- Post-Marketing Surveillance
🌟 Why Join ICON?
- Work with a leading global CRO.
- Exposure to international drug safety projects.
- Career growth in Pharmacovigilance and Drug Safety.
- Learning and development opportunities.
- Global career mobility and advancement.
- Collaborative and inclusive work culture.
💰 Salary Information
Based on current industry standards for Pharmacovigilance Associates and Senior Pharmacovigilance Associates in India, the estimated salary range is:
₹5.5 LPA – ₹9.5 LPA
Actual compensation may vary depending on experience, case processing expertise, coding knowledge, and interview performance.
📈 Career Path
- Drug Safety Associate
- Pharmacovigilance Associate
- Senior Pharmacovigilance Associate
- Drug Safety Specialist
- Senior Drug Safety Specialist
- Pharmacovigilance Team Lead
- Pharmacovigilance Manager
- Global Safety Lead
📝 Resume Tips
- Highlight ICSR processing experience.
- Mention MedDRA and WHO-DD coding expertise.
- Include case processing productivity and quality metrics.
- Showcase literature screening and reconciliation activities.
- Mention Argus, ARISg, or other safety databases.
- Use ATS-friendly Pharmacovigilance keywords.
🎯 Interview Preparation Tips
- Revise ICSR lifecycle and case processing workflow.
- Review seriousness, expectedness, and causality concepts.
- Practice MedDRA coding scenarios.
- Understand expedited reporting timelines.
- Review literature case processing requirements.
- Revise global PV regulations and GVP guidelines.
- Prepare examples of quality review activities.
❓ Common Interview Questions
- Explain the ICSR processing workflow.
- What is the difference between serious and non-serious cases?
- What is MedDRA and why is it used?
- How do you determine case validity?
- What are expectedness and causality assessments?
- How do you process literature cases?
- What is WHO-DD coding?
- How do you perform quality checks on cases?
- What are expedited reporting timelines?
- Why do you want to join ICON?
❓ Frequently Asked Questions (FAQ)
Q1. What experience is required?
Minimum 2 years of Pharmacovigilance and Drug Safety experience.
Q2. Which qualifications are eligible?
B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, Biotechnology, Biochemistry, Microbiology, Nursing, and Healthcare graduates.
Q3. Is MedDRA coding experience required?
Yes, MedDRA coding knowledge is highly preferred.
Q4. What locations are available?
Chennai and Trivandrum.
Q5. Is this suitable for freshers?
No, candidates should have at least 2 years of Pharmacovigilance experience.
📝 How to Apply
- Update your resume with PV case processing experience.
- Highlight MedDRA, WHO-DD, and safety database knowledge.
- Review the complete job description carefully.
- Apply through the official application link.
👉 Step-by-Step Guide: How to Apply for Healthcare & Pharma Jobs
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