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ProductLife Group Hiring Pharmacovigilance Professionals
🏢 ProductLife Group
🌍 Remote India
💊 Pharmacovigilance
📂 Drug Safety
🎓 0–4 Years
ProductLife Group is hiring for Data Officer – Local Safety and Information & Documentation Officer roles under its Safety and Vigilance division.
These remote opportunities are ideal for candidates interested in ICSR Processing, Literature Monitoring, Drug Safety, Pharmacovigilance Operations, Safety Databases, GVP, FDA & EU PV Regulations.
📋 Job Overview
- Company: ProductLife Group
- Roles: Data Officer – Local Safety & Information and Documentation Officer
- Location: Remote India
- Department: Safety and Vigilance
- Industry: Pharmacovigilance / Drug Safety
- Experience: 0–4 Years
- Employment Type: Permanent Contract
- Work Mode: Work From Home
💰 Estimated Salary Range: ₹4 – ₹9 LPA
🏢 About ProductLife Group
ProductLife Group is a globally recognized healthcare and life sciences organization specializing in pharmacovigilance, regulatory affairs, quality compliance, and drug safety services.
The company provides strong global exposure in international pharmacovigilance operations, safety monitoring, literature surveillance, and regulatory compliance.
💊 Data Officer – Local Safety (Pharmacovigilance)
💰 Estimated Salary: ₹5 – ₹9 LPA
📌 Key Responsibilities
- Perform local safety case processing and data entry
- Conduct ICSR quality control and follow-up activities
- Manage safety email inboxes and vigilance cases
- Coordinate with healthcare professionals and reporters
- Support pharmacovigilance reconciliations
- Participate in audits, inspections, and CAPA activities
- Support local PV department operations
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Pharm.D
- Life Sciences / Nursing / Healthcare Fields
- Minimum 2 Years PV Experience Preferred
- Knowledge of FDA, EU PV, GVP & GCP preferred
⭐ Required Skills
- ICSR processing knowledge
- Safety database exposure
- Quality control understanding
- Strong communication skills
- Attention to detail and teamwork
📚 Information & Documentation Officer
💰 Estimated Salary: ₹4 – ₹7 LPA
📌 Key Responsibilities
- Conduct literature searches in international databases
- Perform literature watch activities
- Use PubMed and ADIS databases for case identification
- Support quality control implementation
- Manage client document storage and tracking
- Participate in audits and compliance activities
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Pharm.D
- Life Sciences Graduates
- 1–3 Years PV Experience Preferred
- Freshers with PV Training may also apply
⭐ Preferred Skills
- PubMed and literature monitoring knowledge
- Understanding of GVP Module VI
- Pharmacology basics
- MS Office and SharePoint proficiency
- Strong English communication skills
🌍 Benefits of Working at ProductLife Group
- Remote work flexibility
- Global exposure in drug safety operations
- Experience with FDA and EU PV regulations
- International client exposure
- Career growth in Pharmacovigilance
- Learning opportunities in literature monitoring and ICSR processing
📄 Resume Tips for Pharmacovigilance Roles
- Highlight ICSR processing and literature monitoring exposure
- Mention GVP, FDA, and EU PV knowledge clearly
- Add safety database and QC experience
- Include PubMed or literature search experience
- Showcase communication and documentation skills
- Keep your resume ATS-friendly and concise
📚 Resume & Career Resources
👉 Pharmacy Career Guide
👉 Healthcare Knowledge Hub
🎯 Interview Tips
- Revise ICSR workflow and literature monitoring basics
- Understand GVP Module VI concepts
- Prepare MedDRA and safety database concepts
- Review FDA and EU PV guidelines
- Practice communication and case handling scenarios
- Be ready for QC and compliance-based questions
📚 Interview Preparation Resources
👉 Healthcare Interview Questions
👉 Aptitude & Reasoning Quiz
👉 Explore Healthcare Quizzes
📝 How to Apply for Healthcare & Pharma Jobs
🚀 Job Application Link
🚀 Apply: Data Officer – Local Safety (Pharmacovigilance)
🚀 Apply: Information & Documentation Officer
📌 Important Note Before You Apply:
Please make sure to read the complete job description carefully before submitting your application. Understanding ICSR processing, literature monitoring, GVP guidelines, and drug safety workflows significantly improves your chances of selection.
Please make sure to read the complete job description carefully before submitting your application. Understanding ICSR processing, literature monitoring, GVP guidelines, and drug safety workflows significantly improves your chances of selection.
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