Pharmacovigilance Case Processor Job 2026 in Gurugram | ESS Pharma Jobs for Freshers
Pharmacovigilance Case Processor Job 2026 in Gurugram | ESS Pharma Jobs for Freshers
(Pharmacovigilance Case Processor Job 2026)
(Pharmacovigilance Case Processor Job 2026)
Introduction
If you are planning to build a career in pharmacovigilance and drug safety, this opportunity can be a perfect starting point. Elite Safety Sciences (ESS) is hiring Pharmacovigilance Case Processors in Gurugram for candidates with 0–3 years of experience. With increasing demand for drug safety professionals globally, this role provides hands-on exposure to real-world pharmacovigilance processes such as ICSR handling, adverse event reporting, and safety database management.
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About The Company
Elite Safety Sciences (ESS) is a growing pharmacovigilance and drug safety services company specializing in clinical safety, regulatory compliance, and risk management solutions. The company is headquartered in India (Gurugram, Haryana) and operates with a focus on global pharmacovigilance standards. ESS supports pharmaceutical companies, CROs, and healthcare organizations in maintaining drug safety and compliance. With a skilled workforce and expanding client base, the company offers strong career growth opportunities in clinical research and pharmacovigilance. It has been operating for several years and is steadily building its presence in the global drug safety industry with a team of trained professionals.
Job Overview Summary
The Pharmacovigilance Case Processor role at ESS is designed for freshers and early-career professionals who want to enter the drug safety domain. The role involves working on Individual Case Safety Reports (ICSRs), medical coding, and safety data analysis. Candidates will gain exposure to both clinical trial and post-marketing safety data, making it a strong foundation for a long-term career in pharmacovigilance and regulatory affairs.
Vacancy Details (Official)
- Company Name: Elite Safety Sciences (ESS)
- Role: Pharmacovigilance Case Processor
- Location: Gurugram, Haryana, India
- Experience: 0–3 Years
- Qualification: B.Pharm / M.Pharm / PharmD
- Industry: Pharmacovigilance / Drug Safety / Clinical Research
Responsibility Explanation
In this role, you will be responsible for handling drug safety data and ensuring accurate reporting of adverse events. Your main work will involve processing ICSRs collected from different sources, such as clinical trials and post-marketing surveillance.
You will perform medical coding using standard dictionaries like MedDRA and WHO-DD, ensuring proper classification of medical terms and drugs. Writing clear and medically accurate narratives for each case is also a critical part of the job.
Additionally, you will generate and manage safety queries, follow up with healthcare professionals and clinical trial sites, and ensure all information is complete and compliant with global pharmacovigilance regulations. This role gives you full exposure to end-to-end PV workflows, which is highly valuable for future career growth.
Eligibility (Official)
- B.Pharm / M.Pharm / PharmD graduates
- 0–3 years of experience in pharmacovigilance or related field
- Basic understanding of drug safety and adverse event reporting
Skills Required
To succeed in this role, candidates should have a strong understanding of pharmacovigilance concepts and drug safety processes. Knowledge of ICSR processing, medical terminology, and safety databases is important.
Good English communication skills are essential, especially for writing case narratives and communicating with global teams. Attention to detail is critical because even small errors in safety data can impact regulatory compliance. Candidates should also be quick learners and willing to adapt to new tools and workflows.
Salary Estimate
The expected salary for this role ranges between ₹3.0 LPA and ₹5.5 LPA, depending on skills, qualifications, and interview performance. Freshers with strong pharmacovigilance knowledge and certifications may get better offers. The role also provides long-term growth opportunities in high-paying domains like drug safety and regulatory affairs.
Interview Details (Official)
- Interview Mode: Virtual / Online
- Rounds:
- HR Screening
- Technical Interview (Pharmacovigilance basics, ICSR)
- Final Discussion
- Shortlisted candidates will be contacted via email
Required Documents
Candidates should prepare the following documents:
- Updated Resume (ATS-friendly)
- Educational Certificates
- ID Proof (Aadhar / PAN)
- Passport Size Photo
- Pharmacovigilance Certification (if available)
- Internship or Experience Certificates (if any)
How to Apply (Clean Method)
Interested candidates can apply by sending their updated CV to:
Subject Line: Application for Case Processor – Pharmacovigilance
FAQs Section
Q1. Who can apply for this job?
Candidates with B.Pharm, M.Pharm, or PharmD qualifications can apply.
Q2. Is this job suitable for freshers?
Yes, freshers with 0–3 years of experience can apply.
Q3. What is ICSR in pharmacovigilance?
ICSR stands for Individual Case Safety Report, used to report adverse drug events.
Q4. What is the salary range?
The salary ranges between ₹3.0 and ₹5.5 LPA.
Q5. Is experience mandatory?
No, freshers can apply, but basic knowledge is required.
Final Conclusion
This Pharmacovigilance Case Processor job at ESS is an excellent opportunity for freshers and early-career professionals to enter the high-demand field of drug safety. With hands-on experience in ICSR processing, medical coding, and global safety workflows, this role can build a strong foundation for a successful career in pharmacovigilance and clinical research. Candidates looking for pharma jobs in Gurugram should not miss this opportunity.
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Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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