Non-Clinical Job at Novo Nordisk
A rare opportunity has emerged for experienced professionals to join Novo Nordisk as a Safety Surveillance Specialist in Bangalore. This Non-Clinical Job is pivotal in ensuring the safety profile of Novo Nordisk products across various therapeutic areas, including Diabetes, Obesity, and Rare Diseases. Interested candidates are encouraged to apply before the deadline on 26 October 2026.
About Novo Nordisk:
Novo Nordisk is a global healthcare company with a strong focus on diabetes care, obesity management, and rare diseases. Headquartered in Denmark, the company is renowned for its commitment to innovative treatments and patient safety. With a presence in multiple countries, Novo Nordisk strives to improve the lives of people living with chronic conditions through advanced medical solutions and dedicated research.
Job Details:
- Department: Global Patient Safety, Novo Nordisk Global Business Services (GBS)
- Location: Bangalore, Novo Nordisk Global Business Services (GBS), India
- Application Deadline: 26 October 2026
Job Description:
As a Safety Surveillance Specialist, the successful candidate will play a crucial role in establishing and protecting the safety profile of Novo Nordisk products. This involves analyzing data from clinical trials, spontaneous reports, literature, and post-marketing sources to derive clear safety strategies and benefit-risk conclusions. The role requires a strong medical judgment to identify concerns early and maintain accurate safety information throughout each product’s lifecycle.
Key Responsibilities:
- Accountable for the medical safety evaluation of products from clinical development through to the market, transforming complex data into clear decisions and documented conclusions.
- Establish and maintain the product safety profile through critical safety data analysis, including signal detection, evaluation, and expert interpretation of literature.
- Lead pharmacovigilance planning by developing and executing safety strategies to evaluate safety issues throughout the product lifecycle.
- Provide expert opinion on benefit-risk assessments and contribute to risk management strategies.
- Contribute to clinical study designs and the safety monitoring strategy of study protocols.
- Support the development and maintenance of core reference safety information, participate in product labeling, and ensure accurate documentation in regulatory reports.
- Establish and contribute to safety governance meetings, representing Safety Surveillance in discussions with regulatory authorities, external consultants, and partners.
Eligibility Criteria for the Non-Clinical Job:
- A medical degree (MBBS or MD) from an accredited institution.
- A minimum of 12 years in pharmacovigilance or patient safety, with proven delivery.
- Extensive experience in signal management, risk management plans (RMPs), and aggregate safety reports.
- A strong understanding of drug development and regulatory frameworks.
- The ability to interpret epidemiological data and synthesize evidence into sound conclusions.
- Strong project and stakeholder management skills.
- Excellent written and spoken communication skills, with fluency in English.
- An innovative mindset, with a track record of contributing to long-term strategy and process improvements.
This Safety Surveillance Specialist job at Novo Nordisk represents a significant opportunity for qualified professionals to influence the safety strategies of vital medical products. Candidates with the required expertise are encouraged to apply before the deadline on 26 October 2026 to contribute to the safety and well-being of patients globally.
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