Corporate Pharmacovigilance Job at Novo Nordisk
Are You an MD Graduate Looking for a Career in Global Pharmacovigilance? If you’re passionate about drug safety, pharmacovigilance, and patient care beyond clinical practice, this could be your next career opportunity. Novo Nordisk is hiring a Safety Surveillance Adviser for its Global Patient Safety team in Bengaluru. This Corporate Pharmacovigilance Job in Bengaluru offers the chance to work on global safety surveillance, risk management, regulatory reporting, and clinical development while collaborating with international teams.
About the Company:
Novo Nordisk is a globally recognized healthcare company with over 100 years of experience in developing innovative treatments for chronic diseases. Headquartered in Denmark, the company is a leader in diabetes care and has expanded its expertise into obesity, rare diseases, and other serious chronic conditions. With a strong commitment to innovation, patient safety, and scientific excellence, Novo Nordisk continues to improve the lives of millions of people worldwide through groundbreaking healthcare solutions.
Job Details:
- Job Title: Safety Surveillance Adviser
- Department: Global Patient Safety (GPS)
- Category: Regulatory Affairs & Safety Pharmacovigilance
- Location: Bengaluru (Bangalore), Karnataka, India
- Employment Type: Full-Time
- Application Deadline: 31 July 2026
Key Responsibilities:
- Establish and maintain the safety profile of Novo Nordisk products during development and post-marketing phases.
- Perform continuous safety surveillance using global safety data from worldwide sources.
- Monitor and communicate drug safety issues internally and to Health Authorities.
- Chair and manage cross-functional product safety committees throughout the product lifecycle.
- Maintain and update the Company Core Data Sheet (CCDS) and marketed product labeling in this Corporate Pharmacovigilance Job in Bengaluru.
- Review Labeling Change Requests (LCRs) and provide safety-related recommendations.
- Prepare Development Safety Update Reports (DSURs), Periodic Safety Update Reports (PSURs), SUSAR reports, and Risk Management Plans (RMPs).
- Respond to safety-related queries from Health Authorities and Novo Nordisk affiliates.
- Provide safety input for Product Development Plans, clinical trial protocols, Clinical Study Reports, Investigator’s Brochures, integrated safety summaries, abstracts, and scientific publications at Novo Nordisk Careers.
- Participate in project teams and clinical trial groups to provide proactive safety guidance.
- Conduct investigator safety training when required.
- Support Data Monitoring Committees (DMCs), Ethics Committees (ECs), and Health Authorities with safety-related documentation and responses.
- Ensure patient safety throughout the clinical development lifecycle.
Educational Requirements for the Corporate Pharmacovigilance Job:
- Master’s in Medicine or MD (Post MBBS) is preferred.
- Relevant experience in Signal Management, Aggregate Safety Reporting, and Individual Case Safety Reports (ICSR).
- Prior experience in Pharmacovigilance or Drug Safety is preferred.
Skills Required:
- Strong knowledge of Pharmacovigilance and Drug Safety.
- Experience in Signal Management.
- Knowledge of Aggregate Safety Reporting (DSUR, PSUR, SUSAR, RMP).
- Experience with Individual Case Safety Reports (ICSR).
- Understanding of clinical trial safety monitoring.
- Familiarity with regulatory guidelines and Health Authority requirements.
- Excellent analytical and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to collaborate with global cross-functional teams.
- Strong organizational and stakeholder management skills.
- Proficiency in Microsoft Outlook, Word, Excel, and PowerPoint.
- Ability to adapt quickly in a dynamic and fast-paced work environment.
Benefits of the Corporate Pharmacovigilance Job:
- Join a globally recognized leader in diabetes, obesity, and rare disease research.
- Work with the Global Patient Safety team on international pharmacovigilance projects.
- Gain exposure to global regulatory authorities and drug safety reporting.
- Collaborate with multidisciplinary teams across India and Denmark.
- Contribute to patient safety throughout the lifecycle of innovative medicines.
- Develop expertise in signal detection, safety surveillance, and risk management.
- Work in a collaborative, inclusive, and innovation-driven environment.
- Access continuous learning and professional development opportunities.
- Build a rewarding career with one of the world’s most respected pharmaceutical companies.
- Be part of an organization committed to improving global healthcare and patient outcomes.
