Looking to grow your career in pharmacovigilance (PV) and drug safety? ProPharma is hiring a Pharmacovigilance Scientist in India for its Benefit-Risk team. This remote opportunity is ideal for professionals with 2+ years of PV experience, especially in aggregate safety report writing, signal detection, and risk management.
With increasing global demand for drug safety scientists, this role offers strong exposure to ICH guidelines, regulatory writing, and global pharmacovigilance operations.
๐ Job Overview โ Pharmacovigilance Scientist
- Company: ProPharma
- Role: Pharmacovigilance (PV) Scientist
- Location: India (Remote; Hyderabad preferred)
- Experience: 2+ Years
- Job Type: Full-Time
- Department: Benefit-Risk / Pharmacovigilance
๐งช Key Responsibilities
As a Pharmacovigilance Scientist, you will:
- Author aggregate safety reports:
- PSURs / PBRERs
- PADERs / Annual Reports
- DSURs
- Prepare and maintain Risk Management Plans (RMPs)
- Contribute to signal detection and signal management reports
- Perform literature search, screening, and case validation
- Conduct duplicate checks and safety data extraction
- Generate and review line listings (LLs) from safety databases
- Support regulatory compliance (ICH, FDA, EMA)
- Participate in audits, inspections, and CAPA activities
- Collaborate with global teams on pharmacovigilance operations
๐ Qualifications & Eligibility
Education:
- Bachelorโs / Masterโs degree in:
- Pharmacy (B.Pharm / M.Pharm)
- Nursing
- Life Sciences
- Related healthcare field
Experience:
- Minimum 2+ years in pharmacovigilance
- Hands-on experience in:
- Aggregate report writing (PSUR, DSUR, PBRER)
- Literature screening & signal detection
- Medical writing in PV
๐ง Required Skills
- Strong analytical and problem-solving skills
- Excellent medical writing & communication
- Knowledge of global PV regulations (ICH-GCP, FDA, EMA)
- Experience with safety databases & literature tools
- High attention to detail and quality compliance
๐ผ Salary & Benefits
- Estimated Salary: โน6,00,000 โ โน10,00,000 per annum (industry benchmark for 2โ4 yrs PV experience)
- Remote work flexibility
- Exposure to global pharmacovigilance projects
- Career growth in drug safety & regulatory science
- Inclusive and collaborative work culture
๐ Why This Role is in Demand
The demand for pharmacovigilance scientists in India is rapidly increasing due to:
- Expansion of clinical trials and drug approvals
- Strict global regulatory requirements
- Growth in outsourcing (CROs like ProPharma)
This role strengthens your profile in aggregate reporting, signal management, and benefit-risk evaluation, which are highly valued skills globally.
๐ฉ How to Apply
