Pharmacovigilance Jobs at ProPharma Careers | Life Science Jobs | Apply Now
If you’re searching for high-impact Pharmacovigilance Jobs, this opportunity at ProPharma Careers could be your breakthrough role. ProPharma is hiring a Pharmacovigilance Safety Scientist in Bangalore for experienced professionals in drug safety, aggregate report writing, and regulatory compliance. Among the most competitive Life Science Jobs in India, this role offers exposure to global regulatory frameworks including ICH-GCP, FDA, and EMA guidelines while working in a dynamic onsite/hybrid model.
- Position Title: Pharmacovigilance Safety Scientist
- Job Requisition ID: JR 7763
- Location: Bangalore
About the Company:
For over 20 years, ProPharma has improved patient health and wellness by providing expert advisory and consulting services to biotech, medical device, and pharmaceutical organizations worldwide. Through its advise-build-operate model, the company supports clients across the complete product lifecycle. Under ProPharma Careers, professionals gain exposure to regulatory sciences, clinical research solutions, pharmacovigilance, quality & compliance, medical information, and R&D technology services.
Job Details:
The Pharmacovigilance (PV) Safety Scientist supports the Benefit-Risk group by ensuring operational pharmacovigilance activities are executed with quality and regulatory compliance. This role within Pharmacovigilance Jobs involves authoring aggregate reports such as PSURs, PBRERs, PADERs, DSURs, and Risk Management Plans (RMPs). The candidate will coordinate with senior PV scientists and management while ensuring timely submission of deliverables to global health authorities. This is a full-time position based in Bangalore under ProPharma Careers, offering onsite/hybrid flexibility.
Key Responsibilities:
- Author Aggregate Reports (PSURs, PBRERs, PADERs, DSUR)
- Prepare Risk Management Plans (RMPs)
- Author Signal Management Reports
- Conduct literature search and validity checks
- Extract and validate safety data
- Generate Line Listings from safety databases
- Reconcile relevant trackers
- Support high-priority ad-hoc pharmacovigilance activities
- Ensure compliance with ICH-GCP, FDA, EMA, and global PV regulations
- Maintain quality standards within deliverables
Educational Requirements:
- Bachelor/master’s degree in Life Science, or other health-related field, or equivalent qualification/work experience.
Skills Required:
- Strong analytical and problem-solving skills
- Excellent medical writing ability
- Knowledge of global pharmacovigilance regulations
- Understanding of ICH-GCP, FDA, EMA frameworks
- Experience in literature screening and aggregate report authoring
- Ability to analyze large volumes of safety data
- Strong organizational skills and attention to detail
- Proficiency in MS Office and web-based applications
- Ability to work in a matrix and global environment
If you’re aiming to grow in global drug safety and regulatory sciences, this is one of the most promising Pharmacovigilance Jobs available today. With strong exposure under ProPharma Careers and a structured work environment, this role stands out among premium Life Science Jobs in India. Apply now and take the next step toward a stable and rewarding pharmacovigilance career.
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