India's DMPLOI - Jobs & Networking App
Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full-Time | Regular
Job ID: R-89283
Lilly is on a mission to unite caring with discovery to improve life for people around the world. With a legacy of innovation and a strong foundation in global healthcare, Lilly is seeking a highly skilled and motivated Clinical Surveillance Scientist to join the Global Patient Safety (GPS) team in Bangalore.
Clinical Surveillance Scientist
About the Role
As a Clinical Surveillance Scientist, you will play a critical role in ensuring patient safety by analyzing clinical and safety data, identifying potential risks, responding to regulatory inquiries, and contributing to global regulatory reporting. This role demands strong scientific acumen, effective decision-making, and collaborative communication across global functions.
Key Responsibilities
Signal Detection & Safety Evaluation
- Identify and assess safety signals from multiple data sources.
- Conduct evaluations that impact product labels and benefit-risk profiles.
- Collaborate with safety physicians, epidemiologists, and scientists.
- Lead safety discussions and document safety-related outcomes.
Regulatory & Risk Management
- Author and contribute to regulatory reports such as DSURs, PSURs, PBRERs, and RMPs.
- Assist in responding to global regulatory authority inquiries.
- Support labeling changes and medical communication content.
Cross-functional Collaboration
- Communicate safety findings to internal stakeholders and teams.
- Foster effective working relationships across safety, clinical, regulatory, and legal functions.
- Mentor junior team members and promote continuous improvement in pharmacovigilance practices.
Qualifications
Education and Experience (Any of the following):
- Advanced degree in a medical/scientific field (PharmD, PhD, Clinical Nurse Specialist, etc.) with 1–3 years of relevant experience.
- Bachelor’s degree with 7–10 years of experience in the pharmaceutical industry or clinical development.
- 3–5 years of clinical or pharmaceutical experience, including at least 2 years in clinical development.
Preferred Skills:
- Deep understanding of pharmacovigilance and safety reporting regulations.
- Clinical knowledge in pharmacology, physiology, and disease states.
- Ability to manage multiple tasks and communicate effectively in cross-functional teams.
Why Lilly?
At Lilly, we don’t just create medicines — we create better lives. Working here means joining a global team dedicated to innovation, integrity, and inclusivity. Our values are reflected in how we care for our employees, partners, and the patients we serve.
Be part of a company where you can grow, innovate, and contribute to meaningful change in global health.
Apply now and help make life better for people around the world.
Quick Details:
- Position: Clinical Surveillance Scientist
- Company: Eli Lilly
- Location: Bangalore, India
- Job Type: Full-Time | Regular
- Job ID: R-89283
