IQVIA Hiring Safety Associate (Pharmacovigilance) - Kolkata & Kochi
Are you seeking high-paying IQVIA Careers India or Safety Associate Jobs? Globally recognized clinical research leader IQVIA is hiring experienced Safety Associate (Pharmacovigilance) professionals. The openings are available at Kolkata (West Bengal) and Kochi (Kerala), offering a stable 5-day office-based work model.
Selected candidates will perform end-to-end Individual Case Safety Reports (ICSRs) processing on the Argus Safety database and code adverse events. To prepare your CV details, check out our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | Safety Associate |
| Company | IQVIA |
| Locations | Kolkata (West Bengal) & Kochi (Kerala), India |
| Work Mode | 5 Days, Office-Based (Kolkata local candidates preferred) |
| Employment Type | Full-Time |
| Experience Required | 1 to 2.5 Years |
| Qualifications | B.Pharm, M.Pharm, Pharm.D |
| Department | Pharmacovigilance (PV) / Drug Safety Operations |
| Salary Package | ₹3.2 - ₹5.5 LPA (Expected, based on skills) |
| Application Mode | Email Application |
💼 Key Responsibilities
- Perform end-to-end pharmacovigilance (PV) case processing of adverse event reports.
- Review, analyze, and process Individual Case Safety Reports (ICSRs) from various sources.
- Code adverse events and medical terms using MedDRA and WHO Drug dictionaries.
- Ensure complete compliance with global pharmacovigilance regulations and guidelines.
- Work hands-on with the Argus Safety database to enter and track safety reports.
- Maintain high standards of data quality and meet strict regulatory timelines for safety reporting.
- Participate in team meetings and support quality audits or inspections as required.
Understanding salary standards and growth paths is crucial in drug safety careers. To see how PV salaries scale between India and international regions, read our analysis on Pharmacovigilance Salary: India vs USA.
🎓 Eligibility & Qualifications
Candidates applying for this Safety Associate position must meet the following:
- Education: Bachelor's or Master's degree in Pharmacy (B.Pharm / M.Pharm) or Pharm.D.
- Experience: Minimum 1 to 2.5 years of hands-on experience in pharmacovigilance case processing.
- Technical Skill: Mandatory hands-on experience using the Argus Safety Database.
- Location: Candidates must be based in Kolkata (for Kolkata location, West Bengal localites only).
For pharmacy graduates planning long-term career goals after graduation, check out our comprehensive analysis on B.Pharm Careers: India vs USA.
Additional Requirements
- Strong understanding of ICSR processing workflows and medical terminology.
- Familiarity with GVP (Good Pharmacovigilance Practices) and ICH guidelines.
- Excellent written and verbal communication skills.
- Strong analytical abilities and detail-oriented mindset.
💰 Salary & Employee Benefits
- Estimated salary of ₹3.2 – ₹5.5 LPA matching industry standards for mid-level drug safety roles.
- Direct exposure to global pharmacovigilance projects and international clinical trials safety.
- Structured 5-day office work model.
- Excellent learning environment within a world-leading CRO.
To test and improve your drug safety and clinical operations compliance knowledge, try our interactive Clinical Trial Assistant (CTA) Quiz.
🌟 Why Join IQVIA?
- IQVIA is a global leader in clinical research, health data analytics, and pharmacovigilance operations.
- Provides structured training programs to help you scale into senior case processor or quality reviewer roles.
- Offers exposure to advanced drug safety databases and global reporting platforms.
📑 Resume Tips for PV Roles
- Highlight your case processing volume and experience with the Argus Safety database.
- Mention your expertise in coding systems such as MedDRA and WHO Drug dictionaries.
- Tailor your resume format to highlight quality metrics and timeline compliance achievements.
🎯 Safety Associate (PV) Interview Questions
- What are the four minimum criteria required for a valid adverse event case?
- What is MedDRA and explain its hierarchy from LLT to SOC.
- How do you distinguish between serious and non-serious adverse events?
- Explain the terms "expedited reporting" and "periodic safety reporting".
- How do you perform duplicate search checks in a safety database?
For a detailed list of common questions asked during PV interviews, check out our guide on Top 100 Entry Level Pharmacovigilance Questions.
📧 How to Apply?
Interested and eligible candidates can apply by sharing their updated CV directly with the IQVIA recruitment team at the following email addresses:
- Recruiter Email 1: heena.gill@iqvia.com
- Recruiter Email 2: sherry.thammappakm@iqvia.com
Please ensure you use the subject line: "Application for Safety Associate (Pharmacovigilance)" when sending your email.
🚀 Apply Now
Apply via Email❓ Frequently Asked Questions
Q. Who is eligible to apply?
B.Pharm, M.Pharm, and Pharm.D graduates with 1 to 2.5 years of PV experience.
Q. Is the Argus Safety database experience mandatory?
Yes, hands-on experience using the Argus database is a mandatory requirement.
Q. What is the work model?
This is a 5-day office-based full-time position located in Kolkata & Kochi.
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