Data Officer (Pharmacovigilance)
ProductLife Group (PLG) is hiring Data Officers (Pharmacovigilance) for its Remote India team. This work-from-home opportunity is ideal for professionals with experience in Pharmacovigilance, Drug Safety, ICSR Processing, EudraVigilance, MedDRA Coding, and Regulatory Submissions.
Candidates looking to build a career in global pharmacovigilance operations while working remotely are encouraged to apply.
📋 Job Overview
| Particular | Details |
|---|---|
| Company | ProductLife Group (PLG) |
| Position | Data Officer (Pharmacovigilance) |
| Location | Remote India |
| Employment Type | Full-Time |
| Work Mode | 100% Remote |
| Qualification | B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, Life Sciences or related field |
| Experience | 1–3 Years |
💼 Key Responsibilities
- Manage generic and client-specific vigilance email inboxes.
- Perform initial case intake, registration, and duplicate checks.
- Conduct case triage, seriousness assessment, and MedDRA coding.
- Draft case narratives and ensure patient data anonymization.
- Handle case follow-ups, acknowledgements, and closures.
- Submit ICSRs to regulatory authorities, ethics committees, partners, and affiliates.
- Generate line listings, summary tabulations, and database queries.
- Perform EudraVigilance ICSR downloads, MLM searches, and submissions.
- Manage XEVMPD updates and submissions.
- Support MHRA, FDA, and other regulatory authority submissions.
- Prepare Safety Management Plans (SMPs), SOPs, and client templates.
- Generate KPI reports and support audits and inspections.
🎓 Eligibility Criteria
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Other related Life Sciences qualifications.
- 1–3 years of Pharmacovigilance or Drug Safety experience.
🧠 Required Skills
- Pharmacovigilance
- Drug Safety
- ICSR Processing
- MedDRA Coding
- EudraVigilance
- MHRA & FDA Submissions
- Safety Databases
- Regulatory Compliance
- Documentation & Reporting
- Analytical Skills
- Communication Skills
- Remote Collaboration
This role provides the opportunity to work remotely on global pharmacovigilance projects, manage safety data, support international regulatory submissions, and build expertise in worldwide drug safety operations.
💰 Salary & Benefits
Based on the information provided for this position:
Estimated Salary: ₹6.0 – ₹10.0 LPA
Actual compensation may vary depending on experience, skills, and company policies.
Employee Benefits
- 100% Remote Work Opportunity.
- Exposure to Global Pharmacovigilance Projects.
- Career Growth in Drug Safety & Regulatory Affairs.
- Opportunity to work with International Regulatory Authorities.
- Continuous Learning & Professional Development.
- Compliance-focused Global Work Environment.
🌟 Why Join ProductLife Group (PLG)?
- Work with a leading global life sciences consultancy.
- Gain exposure to worldwide pharmacovigilance operations.
- Develop expertise in EudraVigilance and regulatory submissions.
- Collaborate with international safety teams.
- Build experience in global safety databases and compliance.
- Enjoy the flexibility of working remotely.
📈 Career Growth Opportunities
- Senior Pharmacovigilance Data Officer
- Drug Safety Associate
- ICSR Specialist
- Pharmacovigilance Scientist
- Regulatory Affairs Associate
- Safety Database Specialist
- Pharmacovigilance Team Lead
- Drug Safety Manager
📑 Resume Tips
- Highlight Pharmacovigilance and Drug Safety experience.
- Mention ICSR processing and MedDRA coding knowledge.
- Include EudraVigilance and regulatory submission experience.
- Showcase experience with safety databases.
- Mention SOPs, KPI reporting, and documentation skills.
- Keep your resume ATS-friendly.
🎯 Interview Questions
- What is Pharmacovigilance?
- Explain the ICSR lifecycle.
- What is MedDRA coding?
- What is EudraVigilance?
- How do you perform duplicate checks?
- What are MHRA and FDA safety submissions?
- How do you ensure regulatory compliance?
- Why do you want to join ProductLife Group?
- Tell us about your Drug Safety experience.
- How do you prioritize multiple safety cases?
📌 How to Apply?
Interested and eligible candidates can apply online through the official ProductLife Group Careers portal.
🚀 Apply Now
Apply on ProductLife Group Careers📚 Related Resources from Medical Jobs India
❓ Frequently Asked Questions
Q. Who can apply for this role?
Candidates with B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc, or other Life Sciences qualifications and relevant Pharmacovigilance experience can apply.
Q. Is this a remote job?
Yes. This is a 100% Remote India opportunity.
Q. What experience is required?
1–3 years of Pharmacovigilance, Drug Safety, or Vigilance Data Management experience.
Q. What are the key skills required?
ICSR Processing, MedDRA, EudraVigilance, Safety Databases, MHRA/FDA Submissions, and Regulatory Compliance.
Q. What is the estimated salary?
₹6.0–₹10.0 LPA (Estimated).
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