PV Jobs in India | Apply Now for Pharmacovigilance Safety Scientist Role at ProPharma Careers!
Join ProPharma as a Pharmacovigilance Safety Scientist in the Benefit Risk group and contribute to advancing patient health and safety. This full-time role in India focuses on authoring aggregate reports, managing risk, and ensuring compliance with global regulatory standards. Ideal for professionals looking for PV Jobs in India with 2+ years of PV experience and strong analytical and medical writing skills.
Job Details:
- Job Title: Pharmacovigilance Safety Scientist – Benefit Risk
- Location: India
- Employment Type: Full-time
- Posted On: Today
- Job Requisition ID: JR 8265
About the Company:
For the past 20 years, ProPharma has empowered biotech, medical device, and pharmaceutical organizations to advance therapies confidently. Through its advise-build-operate model, ProPharma provides end-to-end consulting solutions in regulatory sciences, clinical research, quality, compliance, pharmacovigilance, medical information, and R&D technology, ensuring de-risked and accelerated drug and device programs.
Education & Experience Requirements:
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Education: Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, or related health field, or equivalent qualification/work experience.
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Experience: 2+ years’ experience in Pharmacovigilance with a focus on medical writing and/or literature search and/or signal detection
Key Responsibilities for the Pharmacovigilance Safety Scientist Role:
- Author aggregate reports (PSURs/PBRERs, PADERs, Annual Reports, ACO, DSUR) for local and global Health Authorities.
- Prepare Risk Management Plans (RMPs) and Signal Management Reports.
- Conduct literature searches and validate aggregate reports.
- Reconcile relevant process trackers and extract/validate data (RSI, Sales, previous reports, RMPs, signals).
- Generate Line Listings (LL) from the safety database.
- Support high-priority ad-hoc activities.
- Ensure deliverables meet regulatory requirements and timelines.
Skills Required for the Pharmacovigilance Safety Scientist Role:
- Analytical and problem-solving skills.
- Strong organizational and teamwork abilities.
- Excellent attention to detail and focus on quality.
- Knowledge of ICH-GCP, FDA, EMA, and other global PV regulations.
- Ability to summarize and analyze large datasets concisely.
- Proficiency in MS Office and web-based applications.
- Ability to author/update SOPs, WIs, and handle deviations/CAPAs.
How to Apply for the Pharmacovigilance Safety Scientist Role?
All applications for roles at ProPharma are personally reviewed by a member of the recruitment team. AI screening tools are not used, and applicants receive a response regarding their application outcome. Candidates can apply at ProPharma Careers.
