ICON Hiring Pharmacovigilance Associate & Senior Pharmacovigilance Associate
Global CRO leader ICON Plc is hiring for Pharmacovigilance Associate and Senior Pharmacovigilance Associate positions in Chennai and Trivandrum. This is an excellent opportunity for professionals experienced in ICSR processing, adverse event reporting, drug safety operations, post-marketing surveillance, and clinical trial pharmacovigilance.
📋 Recruitment Overview
| Position | Experience | Location |
|---|---|---|
| Pharmacovigilance Associate | 2+ Years | Chennai / Trivandrum |
| Senior Pharmacovigilance Associate | 4+ Years | Chennai / Trivandrum |
🏢 About ICON
ICON Plc is a leading global healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies worldwide. The company provides clinical development, pharmacovigilance, regulatory, and healthcare consulting services across global markets.
💊 Position 1: Pharmacovigilance Associate
Experience: Minimum 2 Years
Location: Chennai / Trivandrum
📌 Key Responsibilities
- Process Individual Case Safety Reports (ICSRs).
- Manage adverse event reporting activities.
- Perform case triage and database book-in.
- Prepare medical narratives.
- Perform MedDRA coding.
- Perform WHO-DD coding.
- Apply product labeling information.
- Conduct quality review checks.
- Process literature-based safety cases.
- Support reconciliation activities.
- Maintain compliance with PV SOPs.
💡 Required Skills
- ICSR Processing
- MedDRA Coding
- WHO-DD Coding
- Drug Safety Operations
- Adverse Event Reporting
- Case Processing
- Pharmacovigilance Compliance
🛡 Position 2: Senior Pharmacovigilance Associate
Experience: Minimum 4 Years
Location: Chennai / Trivandrum
📌 Key Responsibilities
- Review post-marketing and clinical trial ICSRs.
- Perform pharmacovigilance quality control.
- Support aggregate reports (PSUR/DSUR).
- Analyze safety data and trends.
- Support signal detection activities.
- Mentor junior PV professionals.
- Participate in audits and inspections.
- Support SOP reviews and updates.
- Ensure database integrity.
- Support risk assessment activities.
💡 Required Skills
- Advanced ICSR Processing
- PV Quality Control
- Aggregate Reporting
- Signal Detection
- Safety Data Analysis
- Regulatory Compliance
- Team Mentoring
🎓 Eligible Qualifications
- B.Pharm
- M.Pharm
- PharmD
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Nursing
- Healthcare Graduates
🎯 Who Should Apply?
- Drug Safety Associates
- Pharmacovigilance Professionals
- ICSR Processing Specialists
- Clinical Safety Associates
- PV Quality Review Professionals
- Post-Marketing Surveillance Professionals
- CRO Professionals
💰 Expected Salary & Benefits
Based on current Pharmacovigilance industry benchmarks in India, the estimated salary range is:
- Pharmacovigilance Associate: ₹4.5 – ₹8.5 LPA
- Senior Pharmacovigilance Associate: ₹8.0 – ₹14.0 LPA
Actual compensation may vary depending on experience, technical expertise, and company policies.
🌟 Why Join ICON?
- Work with a leading global CRO.
- Exposure to international pharmacovigilance projects.
- Career growth in Drug Safety and Risk Management.
- Training and professional development programs.
- Flexible work environment.
- Global career advancement opportunities.
- Collaborative and inclusive workplace culture.
- Participation in innovative clinical research programs.
📈 Pharmacovigilance Career Path
- Drug Safety Associate
- Pharmacovigilance Associate
- Senior Pharmacovigilance Associate
- Drug Safety Specialist
- PV Team Lead
- PV Manager
- Associate Director – Pharmacovigilance
- Director – Drug Safety
📝 Resume Tips
- Highlight ICSR processing experience.
- Mention MedDRA and WHO-DD coding knowledge.
- Include adverse event reporting experience.
- Add reconciliation and literature review activities.
- Mention aggregate reporting experience if applicable.
- Showcase audit and inspection readiness activities.
- Use ATS-friendly resume formatting.
📌 Before applying, read:
👉 Healthcare & Pharma Application Guide🎯 Pharmacovigilance Interview Preparation
- Revise ICSR lifecycle and case processing steps.
- Review seriousness, expectedness, and causality concepts.
- Understand MedDRA hierarchy.
- Review WHO Drug Dictionary basics.
- Understand expedited reporting timelines.
- Study PSUR, DSUR, and aggregate reporting concepts.
- Review signal detection and risk management basics.
❓ Common Interview Questions
- What is Pharmacovigilance?
- What is an ICSR?
- Explain MedDRA coding.
- What is WHO-DD?
- Difference between serious and non-serious adverse events?
- What is causality assessment?
- What is signal detection?
- Explain PSUR and DSUR.
- How do you perform quality review of a case?
- Why do you want to join ICON?
📄 Documents Recommended Before Applying
- Updated Resume
- Educational Certificates
- Experience Certificates
- Latest Increment Letter
- Current CTC Details
- Government ID Proof
- Updated LinkedIn Profile
📚 Recommended Resources
👉 Pharmacovigilance Quiz👉 Drug Safety Analyst Quiz
👉 Top 100 Pharmacovigilance Interview Questions
👉 Pharmacovigilance Salary Guide
👉 Healthcare Quiz Collection
❓ Frequently Asked Questions (FAQ)
Q1. Is pharmacovigilance experience mandatory?
Yes. ICON is seeking candidates with relevant PV experience.
Q2. Which locations are hiring?
Chennai and Trivandrum.
Q3. Is ICSR experience required?
Yes. ICSR processing experience is one of the key requirements.
Q4. Are PharmD candidates eligible?
Yes. PharmD candidates with relevant experience are eligible.
Q5. Is aggregate reporting experience required for senior roles?
Yes. Experience with PSUR, DSUR, and safety reporting is advantageous.
🚀 How to Apply
Interested candidates can apply through the official ICON careers portal.
💊 Apply – Pharmacovigilance Associate🛡 Apply – Senior Pharmacovigilance Associate
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