MD Job Opportunity at Novo Nordisk | Apply Now
Looking for an exciting MD job in pharmacovigilance? Novo Nordisk is hiring a Safety Surveillance Adviser in Bangalore. This is a great opportunity for medical professionals to work in global patient safety, contribute to drug safety monitoring, and grow within a leading healthcare company. If you’re exploring Novo Nordisk careers or MD jobs in Bangalore, this role offers international exposure and impactful work.
Job Details
- Job Position: Safety Surveillance Adviser
- Job Location: Bangalore, Karnataka, India
- Department: Global Patient Safety
- Application Deadline: 08th April 2026
About the Company
Novo Nordisk is a global healthcare leader with over 100 years of experience in defeating chronic diseases. The company focuses on diabetes, obesity, and rare diseases, driven by innovation, research, and a commitment to improving patient lives worldwide. With a strong presence in India, Novo Nordisk Global Business Services (GBS) in Bangalore plays a key role in global operations.
About the Department
The Global Patient Safety team at Novo Nordisk in Bangalore is responsible for monitoring and communicating the safety profile of products across their lifecycle. The team works across therapeutic areas such as Diabetes, Obesity, and Rare Diseases, collaborating with global teams including Denmark. This makes it a strong opportunity for those exploring Novo Nordisk careers and MD jobs in Bangalore.
Job Description
As a Safety Surveillance Adviser, you will be responsible for establishment of the product safety profile during development and maintenance of the labelling for marketed products. Furthermore, perform ongoing and systematic surveillance of Novo Nordisk (NN) products during pre-approval and post-approval phases based on safety information from worldwide sources and communication of drug safety issues internally and to health authorities (HAs), as required.
You will be required to establish, operate and chair the NN cross-functional safety committee throughout the lifecycle of the actual product – present analysis and results of the ongoing safety surveillance at pre-defined intervals in order for the safety committee to make endorsements/recommendations. You will be responsible for all areas related to patient safety in clinical trials.
Qualifications
- Masters in Medicine / MD post MBBS graduate is preferred
- Relevant experience in Signal Management, Aggregate Reporting, and ICSR
- Proficiency in Microsoft Office (Outlook, Word, Excel, PowerPoint)
- Ability to adapt quickly in a dynamic work environment
Key Responsibilities
- Act as Owner of the safety sections of the labelling for the evolving Company Core Data Sheet (CCDS) for development products
- Maintenance of labelling for marketed products and participate as labelling change request (LCR) reviewer
- Prepare relevant sections of Development Safety Update Reports (DSURs), SUSAR reports, PSURs, and Risk Management Plans (RMPs)
- Respond to requests from Health Authorities (HAs) and internal stakeholders
- Provide safety input to Product Development Plan (PDP), trial protocols, clinical trial reports, and Investigator’s Brochure (IB)
- Participate in project and trial teams, and conduct investigator training
- Address safety-related queries from Ethics Committees (ECs) and HAs
- Coordinate deliverables with Data Monitoring Committees (DMCs)
Application Process
To apply, candidates must submit their CV online through the official Novo Nordisk careers portal.
