ProductLife Group Pharmacovigilance Jobs 2026 | Remote Data Officer & Drug Safety Case Processing Jobs in India
Are you seeking ProductLife Group Careers or Drug Safety Remote Jobs in India? Global outsourcing provider ProductLife Group (PLG) is hiring experienced Data Officers for its Life Cycle - Safety and Vigilance division.
This permanent remote pharmacovigilance vacancy is ideal for science and pharmacy professionals with 2 or more years of experience in Adverse Event reporting, ICSR data entry, EudraVigilance database queries, and XEVMPD records maintenance. To write a resume detailing your drug safety case processing achievements, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | ProductLife Group (PLG) |
| Position | Data Officer (Vigilance / Safety) |
| Job Type | Permanent |
| Job Location | India (Remote / WFH) |
| Department | Life Cycle – Safety and Vigilance |
| Experience Required | Minimum 2 Years in Pharmacovigilance |
| Qualifications | B.Pharm, B.Sc, M.Sc Life Sciences, Industrial Biology, Chemistry Engineering |
| Application Mode | Online Application |
💼 Key Responsibilities
- Vigilance Data Entry: Perform data entry and processing of Individual Case Safety Reports (ICSRs) into clinical safety databases.
- Quality Checks (QC): Review safety profiles for completeness and conduct quality reviews of safety cases.
- Dossier Submissions: Submit clinical safety cases to global competent health authorities.
- Regulatory Database Queries: Monitor and download ICSR data from European and national portals like EudraVigilance and the MHRA Portal.
- XEVMPD Maintenance: Record, format, and update medicinal product dictionaries and registries in XEVMPD.
- Documentation Drafting: Assist in drafting Technical Agreements, Safety Management Plans, client report templates, and WPDs (Work Process Documents).
- Query Resolution: Prepare follow-up emails and clarification files to obtain missing clinical patient details.
To learn how remote drug safety analyst salaries compare to specialized clinical trial coordinator and medical writer positions, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Experience
- Education: Bachelor's or Master's degree in Pharmacy, Life Sciences, Industrial Biology, Chemistry Engineering, or related scientific fields.
- Experience: Minimum 2 years of experience in pharmacovigilance, specifically performing case processing, data entry, and QC.
- Service-Provider Track: Prior experience working in a CRO (Contract Research Organization) or service provider environment is preferred.
- Regulatory Knowledge: Basic understanding of European Pharmacovigilance Regulations, EU PV guidelines, GCP, GVP, FDA, and global adverse event guidelines.
- Language Skills: Excellent verbal and written English communication, detailing clinical safety profiles clearly.
For science graduates evaluating safety data analytics pathways compared to conventional lab formulation roles, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join ProductLife Group?
- 100% remote working model, allowing you to work from anywhere in India.
- Gain deep exposure to European safety standards, EudraVigilance, and XEVMPD workflows.
- Collaborative international safety team working with top-tier global pharmaceutical companies.
- Stable career progression in regulatory lifecycle and drug safety services.
To test your basic knowledge of drug safety definitions, clinical trial phases, and ICH parameters before your technical interviews, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Data Officer vs Healthcare IT
Vigilance Data Officers manage safety databases, write case reports, and submit safety data to European authorities to ensure compliance, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for PLG PV Candidates
- Highlight EudraVigilance / XEVMPD: If you have worked on registering medicinal products or downloading cases from EudraVigilance, make sure this is prominent on your CV.
- Specify Quality Control: Detail if you have performed peer review, quality check (QC), or medical narrative writing in previous roles.
- Detail Case Types: State if your experience includes spontaneous cases, clinical trial cases, literature reviews, or device safety reports.
💬 ProductLife Group Data Officer Interview Questions
- Q1. What is XEVMPD and why is it used in European pharmacovigilance?
Answer Guidance: XEVMPD (eXtended EudraVigilance Medicinal Product Dictionary) is a registry database maintained by the EMA. Marketing Authorization Holders (MAHs) are required to submit and update details of all authorized drugs in this database to facilitate safety monitoring and regulatory checks. - Q2. What is the difference between a spontaneous case report and a clinical trial case report?
Answer Guidance: A spontaneous report is an unsolicited safety notification from a healthcare professional or consumer regarding a marketed drug. A clinical trial report is structured safety data collected during a controlled clinical study, where causality assessment and investigator reporting protocols are strictly followed. - Q3. Explain the purpose of a Safety Management Plan (SMP).
Answer Guidance: An SMP is a study-specific document that defines the roles, workflows, timelines, communication channels, and databases used to manage, process, and report serious adverse events between the sponsor, CRO, and clinical trial sites.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via ProductLife Group's official careers portal. Click the button below to apply:
Apply Online – ProductLife Group Career Portal❓ Frequently Asked Questions
Q. Is this PLG Data Officer position remote?
Yes, this is a 100% remote (Work From Home) opportunity based anywhere in India.
Q. What is the required experience for this drug safety vacancy?
Candidates should possess a minimum of 2 years of experience in pharmacovigilance (specifically ICSR entry and QC).
Q. Which degrees are eligible to apply?
Candidates holding a Bachelor's degree in Pharmacy, Life Sciences, Industrial Biology, or Chemistry Engineering are eligible to apply.
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