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Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full-Time, Regular
Job ID: R-89283
Eli Lilly and Company, a global healthcare leader headquartered in Indianapolis, is hiring a Clinical Surveillance Scientist in Bangalore. Lilly is committed to uniting care with discovery to make life better for people around the world. With a mission-driven approach, the company strives to develop life-changing medicines, improve disease management, and give back through community initiatives.
If you are passionate about pharmacovigilance, drug safety, and global patient safety, this opportunity offers a platform to grow your expertise and impact lives worldwide.
Purpose of the Role
The Global Patient Safety (GPS) team at Lilly provides scientific, medical, and pharmacovigilance expertise for both pipeline and marketed products. The Clinical Surveillance Scientist will play a vital role in safety signal detection, risk evaluation, regulatory reporting, and effective communication with stakeholders.
Key Responsibilities
Signal Detection & Safety Data Evaluation
- Identify, analyze, and evaluate safety signals from internal and external sources.
- Review and support label changes/modifications with regulatory and legal teams.
- Lead safety team meetings for clinical and marketed products.
- Define methodology for safety data acquisition and author safety reports.
- Collaborate with physicians, scientists, and epidemiologists for aggregate analysis.
- Communicate safety insights to stakeholders in a timely manner.
Risk Assessment & Regulatory Reporting
- Lead safety data analysis and author sections for DSURs, PADER/PAER, PSURs, PBRERs, and RMPs.
- Provide input to safety communications such as labeling updates and HCP letters.
Pharmacovigilance Leadership
- Communicate with global regulatory agencies (FDA, EMA, MHRA, etc.).
- Mentor and coach junior team members.
- Contribute to organizational improvement and innovation.
- Work in cross-functional global teams ensuring compliance with safety regulations.
Minimum Qualifications
- Advanced degree: PharmD, Nursing (CNS/NP), PhD in relevant scientific fields with 1–3 years’ experience.
OR - Bachelor’s in health/science with 7–10 years’ pharmaceutical or clinical trial experience.
OR - 3–5 years clinical/pharma experience, with at least 2 years in clinical development.
Preferred Skills & Experience
- Strong clinical knowledge of disease states, drug effects, and pharmacology.
- Prior experience in Global Patient Safety/Pharmacovigilance preferred.
- Ability to manage multiple deliverables effectively.
- Strong collaboration and communication skills.
Why Join Lilly?
- Work with a global leader in healthcare innovation.
- Contribute to improving patient safety worldwide.
- Be part of an inclusive, collaborative, and mission-driven organization.
- Opportunities for career development and growth in pharmacovigilance and R&D.
