IQVIA Hiring Safety Associate (Pharmacovigilance) – Thane & Kolkata
Are you seeking IQVIA safety associate jobs, pharmacovigilance case processing careers in Kolkata, or drug safety operations vacancies in Thane? Global clinical research and health data analytics leader IQVIA has announced vacancies for the position of Safety Associate at its Kolkata and Thane branches.
This Individual Case Safety Report (ICSR) processing, safety database entry, MedDRA coding, case narrative compilation, literature surveillance, and regulatory compliance reporting vacancy operates under a full-time office model. The positions are open to life sciences, dental, and pharmacy graduates holding B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, or BDS degrees. Candidates must possess 1 to 1.5 years of experience in pharmacovigilance operations. Shortlisted candidates will be evaluated for immediate project placement. To design a professional ATS-friendly resume highlighting your case review volumes, narrative writing structures, or database experience, check our guide on how to apply for healthcare and pharma jobs online.
📋 Job Overview
- Company: IQVIA
- Position: Safety Associate
- Job Requisition ID: R1558468
- Job Locations: Kolkata, West Bengal | Thane, Maharashtra, India
- Employment Type: Full-Time
- Experience: 1 – 1.5 Years in Pharmacovigilance
- Qualifications: Bachelor’s or Master's degree in Pharmacy, Life Sciences, BDS, or related scientific field
- Application Deadline: July 20, 2026
💼 Key Responsibilities
- ICSR Case Processing: Perform end-to-end processing, evaluation, and logging of adverse event (AE) reports.
- Database Entry: Key in clinical and safety information accurately into global drug safety databases.
- Narrative Writing: Write clear, medically sound, and chronologically accurate case summaries (narratives).
- Medical Dictionary Coding: Code medical histories and events using standard MedDRA terms and map suspect drugs with the WHO Drug Dictionary.
- Literature Surveillance: Support literature-based case collection and screening processes in accordance with guidelines.
- Compliance Operations: Follow company SOPs, project guidelines, and global regulatory timelines (FDA, EMA) for safety reporting.
To prepare for pharmacovigilance questions, safety definitions, and case processing workflows, review our guide on Top 100 Pharmacovigilance Interview Questions.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy, Life Sciences, Nursing, Biotechnology, BDS, or equivalent fields.
- Experience Range: Approximately 1 to 1.5 years of active pharmacovigilance experience.
- Database Skills: Practical knowledge of entering and validating data within global safety databases.
- Medical Terminology: Strong understanding of disease processes, human anatomy, and medical coding definitions.
- Communication: Good written and verbal English communication skills with strong attention to detail.
- Agility: Ability to manage multiple priorities and work flexibly in rotational shifts if required by the business.
For professionals interested in exploring standard compensation packages, domain career tracks, and industry values, check our comparison of Pharmacovigilance Salaries in India vs USA.
🎁 Why Join IQVIA?
- Work for a global leader in clinical research services and health data technology.
- Gain direct operational experience with global drug safety databases and international safety standards.
- Access premium scientific training platforms, peer mentoring, and clear career development paths.
- Stable, full-time employment within a collaborative, inclusive global workplace.
To evaluate your drug safety data retrieval skills and clinical definitions before your interviews, try our interactive Pharmacovigilance Assessment Quiz.
📝 Resume Tips for IQVIA Safety Candidates
- Detail Case Types: Specify if your case processing experience covers clinical trial cases, literature cases, or post-marketing source files.
- Mention Key Tools: Clearly name the version of Argus Safety or other drug safety databases you have operated.
- Use Target Keywords: Include terms like ICSR processing, MedDRA coding, Narrative Writing, GVP guidelines, and database validation.
💬 IQVIA Safety Associate Interview Questions
- Q1. What is an Individual Case Safety Report (ICSR) and what are its key components?
Answer Guidance: An ICSR is a standardized document containing information about an adverse event reported in a single patient related to the use of one or more medicines. Its key components include patient demographics, suspect drug details, adverse event descriptions, case narrative, and the reporter’s details. - Q2. How do you assess the seriousness of an adverse event during case entry?
Answer Guidance: I verify if the event meets any of the FDA/ICH seriousness criteria: results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, or is another medically important event. - Q3. Explain the term "Dechallenge" and "Rechallenge" in causality evaluation.
Answer Guidance: "Dechallenge" refers to stopping or reducing the dose of a drug and observing if the adverse event disappears or improves. "Rechallenge" refers to re-administering the drug to the same patient and observing if the adverse event recurs. A positive dechallenge and rechallenge suggest a strong causal relationship.
📖 How to Apply?
Before submitting your application, please read our step-by-step guidance on how to navigate Workday registration portals, fill out profiles, and format your application:
📧 Email Application Process
Send your updated resume directly to the IQVIA talent acquisition team:
- Email Address: sherry.thammappakm@iqvia.com
- Email Subject Format: Application for Safety Associate - [Your Name] - [Years of Experience]
- Email Note: Highlight your current location (Kolkata or Thane) in the body of your email.
🚀 Direct Application Link
In addition to the email submission, you can also submit your application profile through the official IQVIA Workday careers portal:
Apply Online – IQVIA Careers (Safety Associate R1558468)📄 Try Free ATS Resume Analyzer & Builder
Want to build a professional, recruiter-ready resume before applying? Scan your ATS compatibility score and generate an optimized resume instantly:
🚀 Launch Free ATS Resume Tool❓ Frequently Asked Questions
Q. How should I submit my application?
Eligible candidates can apply by emailing their updated resume to sherry.thammappakm@iqvia.com, or by submitting online via the Workday link.
Q. What is the application deadline?
The official application window for this IQVIA Safety Associate vacancy closes on July 20, 2026.
Q. Where are these job openings based?
The positions are based full-time out of IQVIA's offices in Thane, Maharashtra, and Kolkata, West Bengal.
