Pharmacovigilance Jobs In India: ProPharma is Hiring for the Role Pharmacovigilance Safety Scientist – Apply Now
Are you currently looking for Pharmacovigilance Jobs In India? Step into a rewarding career as a Pharmacovigilance Safety Scientist at ProPharma in India, where your expertise will contribute to improving global health outcomes. In this role, you’ll work on critical pharmacovigilance functions such as benefit-risk assessment, safety data analysis, and aggregate report authoring. ProPharma’s commitment to advancing scientific breakthroughs makes it an ideal environment for professionals passionate about drug safety, regulatory compliance, and global healthcare excellence
Job Details:
- Job Title: Pharmacovigilance Safety Scientist
- Location: India
Job Summary:
The Pharmacovigilance (PV) Scientist supports the activities in the Benefit Risk group by ensuring that day-to-day operational activities are completed. The PV Safety Scientist is expected to be professional and diligent and liaise with the director and management group members within the team on any issues, as well as coordinate the work with the senior PV Scientists. The PV Safety Scientist is also expected to lead by example and ensures quality standards are upheld within the company.
About the Company:
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Education:
Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, or a related field, or equivalent experience.
Experience Requirements:
- Minimum 2 years’ experience in Pharmacovigilance with focus on medical writing, literature search, or signal detection.
- Proven experience in authoring aggregate reports, literature screening, and participating in quality discussions
Essential Functions:
- Authoring Aggregate reports (PSURs/PBRERs, PADERs/Annual Reports/ACO/DSUR) for submission to regulatory authorities.
- Creating Risk Management Plans (RMPs) as part of pharmacovigilance activities.
- Preparing Signal Management Reports and performing literature searches and validity checks for aggregate reports.
- Reconciling relevant process trackers and validating data (RSI, Sales, previous reports, RMP, signals).
- Generating Line Listings from safety databases and supporting high-priority ad-hoc projects.
Necessary Skills and Abilities:
- Strong analytical, problem-solving, and organizational skills.
- Ability to collaborate effectively within a professional team environment.
- Excellent attention to detail, quality focus, and familiarity with global PV regulations (ICH-GCP, FDA, EMA).
- Experience analyzing large datasets, authoring SOPs, and managing deviations/CAPAs.
- Proficiency with IT systems, web applications, and Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to write concise, accurate, and scientific medical text.
