✔ Verified by Medical Jobs India
Hiring Pharmacovigilance Scientist
🏢 ProPharma
📍 Remote / Hyderabad
⏳ 2+ Years
💊 Pharmacovigilance
ProPharma is hiring a Pharmacovigilance Scientist for its Benefit-Risk team. This is a remote job opportunity for candidates with 2+ years of experience in pharmacovigilance, especially in aggregate reporting and signal management.
👉 Explore career path: Pharmacovigilance Salary Guide
📋 Job Overview
- Role: Pharmacovigilance Scientist
- Experience: 2+ Years
- Qualification: Pharmacy / Life Sciences / Nursing
- Location: Remote (India)
- Type: Full-Time
📌 Key Responsibilities
- Prepare PSUR, PBRER, DSUR & PADER reports
- Develop Risk Management Plans (RMP)
- Perform signal detection & validation
- Literature review and safety data analysis
- Generate line listings & safety summaries
- Ensure compliance with ICH, FDA, EMA guidelines
💻 Required Skills
- Strong medical writing skills
- Knowledge of pharmacovigilance regulations
- Signal management & literature screening
- Attention to detail & compliance mindset
🎓 Eligibility
- B.Pharm / M.Pharm / Pharm.D / BSc / MSc / Nursing
- Minimum 2+ years PV experience
- Experience in aggregate reporting
🌟 Why Apply?
- Work on global pharmacovigilance projects
- Remote work flexibility
- Strong career growth in drug safety
- Exposure to global regulatory standards
💡 Interview Tips
- Revise PSUR, PBRER, DSUR concepts
- Understand signal detection workflow
- Practice PV Quiz
📌 Tip: Highlight your aggregate reporting experience clearly in your resume
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with pharmacovigilance operations, adverse event case processing, medical evaluation, aggregate safety reporting, and global drug safety compliance standards before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with pharmacovigilance operations, adverse event case processing, medical evaluation, aggregate safety reporting, and global drug safety compliance standards before proceeding.
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