Corporate Healthcare Job at Novo Nordisk
Are you passionate about ensuring the safety of patients worldwide? As a Safety Operations Advisor at Novo Nordisk, you will be at the forefront of evaluating and reporting adverse events from clinical trials and marketed products. This Corporate Healthcare Job in Bangalore requires a meticulous approach to safeguard patient health and maintain regulatory compliance. The position offers a unique opportunity to work in a globally recognised company committed to patient safety and innovation. By joining the team, you will contribute to Novo Nordisk’s mission of driving change to defeat serious chronic diseases.
About Novo Nordisk:
Novo Nordisk is a global healthcare company focused on diabetes care and other serious chronic diseases. Headquartered in Denmark, it operates in more than 80 countries and markets its products in over 170 countries. The company is dedicated to driving change for better health through innovative research and development in pharmaceuticals, particularly in the areas of diabetes, obesity, and rare blood disorders.
Job Details:
- Company: Novo Nordisk, Global Business Services
- Department: Safety Operations, Global Patient Safety
- Location: Bangalore, Karnataka, IN
- Deadline: 5 October 2026
Job Description:
As a Safety Operations Advisor, the selected candidate will play a critical role in safeguarding patients by ensuring the comprehensive evaluation and reporting of adverse events from clinical trials and marketed products worldwide. This position is essential for maintaining Novo Nordisk’s commitment to patient safety and regulatory excellence.
Key Responsibilities:
- Conducting thorough medical interpretation and evaluation of adverse events reported from worldwide sources, including clinical trials and post-marketing surveillance.
- Ensuring compliance with global regulatory requirements for the collection, evaluation, and expedited reporting of serious adverse events to health authorities.
- Performing medical reviews and causality assessments of serious adverse events, determining potential relationships to Novo Nordisk products.
- Participating in clinical project teams to ensure all safety aspects are appropriately addressed from protocol design through trial conduct in the Corporate Healthcare Job in Bangalore.
- Leading cross-functional groups and chairing safety meetings to drive consistency in case handling across projects and geographies at Novo Nordisk Careers.
- Establishing improved methods and sharing best practices to enhance safety deliverables and ensure accurate MedDRA coding.
- Training investigators, clinical safety associates, and affiliate partners on safety data handling and adverse event management.
Eligibility Criteria for the Corporate Healthcare Job:
- Medical degree (MBBS or equivalent) with postgraduate medical qualification preferred.
- Documented experience in drug safety evaluation, pharmacovigilance, or pharmacoepidemiology with strong knowledge of international regulatory requirements (ICH-GCP, EMA, FDA guidelines).
- Comprehensive understanding of clinical manifestations, disease management, and medical treatment across various therapeutic areas.
- Proven ability to perform independent medical causality assessments and make critical decisions regarding drug safety issues.
- Strong analytical and systematic approach with excellent attention to detail and ability to work under tight regulatory timelines.
- Fluency in English (written and spoken) with excellent communication skills for collaborating across cultural and linguistic differences.
- Self-motivated team player with flexibility to manage multiple priorities and ability to train and mentor others.
