Location: Bangalore, Karnataka, India
Department: Global Patient Safety
Company: Novo Nordisk
Job Category: Regulatory Affairs & Pharmacovigilance
Experience Required: 2–5 years (Not suitable for freshers)
About the Company
Novo Nordisk is a globally recognized healthcare leader with over a century of innovation in treating chronic diseases. With a strong presence in diabetes care, obesity management, and rare diseases, the organization is committed to improving patient lives through scientific excellence, global collaboration, and sustainable healthcare solutions.
Job Overview
The Safety Surveillance Adviser plays a critical role in global pharmacovigilance and drug safety operations. This position is responsible for monitoring and evaluating the safety profile of pharmaceutical products across both clinical development and post-marketing phases. The role requires strong expertise in signal detection, aggregate reporting, and regulatory compliance, ensuring patient safety and benefit-risk balance throughout the product lifecycle.
Key Responsibilities
Lead the development and maintenance of product safety profiles during clinical development and post-marketing phases
Own and manage safety sections of Company Core Data Sheet (CCDS) and labeling updates for marketed products
Conduct continuous safety surveillance using global safety data sources and communicate findings to internal stakeholders and health authorities
Author and review critical aggregate safety reports including DSURs, PSURs, SUSAR reports, and Risk Management Plans (RMPs)
Provide strategic safety input into clinical documents such as protocols, investigator brochures, clinical study reports, and product development plans
Chair and manage cross-functional safety committees, presenting safety data and recommendations for decision-making
Collaborate with clinical, regulatory, and medical teams to ensure compliance with global pharmacovigilance regulations
Support regulatory responses to health authorities and ethics committees on safety-related queries
Conduct investigator training and contribute to safety communication strategies across clinical programs
Required Qualifications
MD or Master’s degree in Medicine (Post-MBBS preferred)
2–5 years of experience in Pharmacovigilance, including Signal Management, Aggregate Reporting, and ICSR processing
Strong knowledge of global safety regulations, including ICH guidelines and GVP modules
Proficiency in Microsoft Office tools including Word, Excel, PowerPoint, and Outlook
Excellent analytical thinking, communication, and stakeholder management skills
Ability to adapt in a fast-paced, global, and cross-functional work environment
About the Department
The Global Patient Safety team based in Bangalore is responsible for end-to-end safety surveillance of products across their lifecycle. The team works closely with international stakeholders, including global hubs, to ensure continuous monitoring, evaluation, and communication of safety data. Therapeutic focus areas include diabetes, obesity, and rare diseases, with a strong emphasis on maintaining a positive benefit-risk profile.
Why Join This Role
Opportunity to work in a globally integrated pharmacovigilance environment
Exposure to end-to-end drug safety lifecycle management
High-impact role contributing directly to patient safety and regulatory decisions
Collaborative culture with global cross-functional teams
Strong career growth in signal detection and aggregate safety domains
Application Process
Interested candidates should apply through the official careers portal of Novo Nordisk by submitting an updated CV and required details.
Application Deadline: 25 April 2026
Important Disclaimer
Candidates are advised to remain cautious of fraudulent job offers. Novo Nordisk does not charge any fees or request payments during the recruitment process. All official communication is conducted through verified channels only.
Equal Opportunity Statement
The company is committed to fostering an inclusive workplace and providing equal opportunities to all applicants, regardless of background.
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