ProductLife Hiring PV Case Specialist
A rare chance for experienced Pharmacovigilance professionals to explore ProductLife Group jobs as a Case Specialist (Clinical Trial Cases) in India. This remote opportunity is suitable for qualified doctors and pharmacists with a strong background in clinical trial case processing. Applications are open until 08 September 2026.
About ProductLife Group
ProductLife Group (PLG) is a leading provider of life sciences services, specializing in pharmacovigilance, regulatory affairs, and clinical trial support. With a commitment to safety and compliance, PLG operates globally, helping pharmaceutical and biotechnology companies manage the complexities of drug development and safety monitoring. The organization is dedicated to providing high-quality services that ensure patient safety and regulatory compliance.
Company: ProductLife Group (PLG)
Job Title: Case Specialist (Clinical Trial Cases)
Department: Life Cycle – Safety and Vigilance
Job Location: India
Work Mode: Remote work possible
Employment Type: Permanent
Experience Required: Minimum 4 years
Clinical Trial Case Processing Experience: Minimum 3 years
Qualification: Doctor or Pharmacist by training
Database Skills: SafetyEasy / Oracle Argus preferred
Salary: Estimated ₹8–15 LPA (depending on experience and skills)
ProductLife Group Jobs: Job Description
The Case Specialist (Pharmacovigilance) will contribute to the processing, medical evaluation, quality control, and management of vigilance cases, particularly clinical trial cases. This ProductLife Group job requires strong knowledge of pharmacovigilance regulations, Individual Case Safety Reports (ICSRs), medical assessment, adverse event evaluation, case coding, causality assessment, seriousness assessment, and safety reporting requirements.
Key Responsibilities
- Performing quality control of pharmacovigilance and vigilance cases.
- Conducting medical evaluation of safety reports.
- Processing and entering vigilance case information into databases and client-approved systems.
- Managing data entry activities for clinical trial safety cases.
- Conducting follow-up activities through phone calls and email communication.
- Performing pre-analysis of complex cases before data entry.
- Reviewing and evaluating medical information associated with vigilance cases.
- Performing medical coding according to applicable dictionaries.
Eligibility Criteria
Educational Qualification:
- Doctor by training, or
- Pharmacist by training
Candidates with professional qualifications and relevant backgrounds in areas such as Pharmacy, Medicine, Pharmacovigilance, Clinical Research, Drug Safety, and related life sciences may be relevant depending on whether they meet the employer’s specific professional qualification requirements.
Experience Required:
- A minimum of 4 years of experience working with service providers and performing quality control of safety cases.
- At least 3 years of experience processing clinical trial cases.
- Practical experience in pharmacovigilance case processing and medical evaluation.
Required Skills
- Pharmacovigilance
- Clinical Trial Safety
- Clinical Trial Case Processing
- ICSR Processing
- Safety Case Quality Control
- Medical Evaluation
- Adverse Event Assessment
- Seriousness Assessment
- Causality Assessment
- Medical Coding
- Drug Safety Regulations
- Oracle Argus Safety
- SafetyEasy Database
- Safety Case Follow-up
- Regulatory Compliance
- Microsoft Office
- Database Experience
How to Apply
Interested candidates can apply through the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Conclusion
This ProductLife Group jobs opportunity is ideal for experienced professionals in pharmacovigilance and clinical trial safety. Qualified candidates are encouraged to apply before the deadline of 08 September 2026 to seize this chance to advance their careers in a reputable organization.
