Company: Novo Nordisk
Department: Regulatory Affairs & Safety Pharmacovigilance
Location: Bangalore
Job Type: Full-Time
Experience Required: 2–6 Years
Eligibility: Freshers are not eligible for this role
About the Company
Novo Nordisk is one of the world’s leading healthcare organizations dedicated to defeating chronic diseases including diabetes, obesity, and rare disorders. With more than 100 years of global healthcare excellence, the company continues to innovate in patient safety, clinical development, and pharmacovigilance operations worldwide.
Job Overview
Novo Nordisk is hiring experienced Pharmacovigilance and Drug Safety professionals for the role of Safety Surveillance Adviser within the Global Patient Safety team in Bangalore. This role focuses on safety surveillance, signal management, aggregate reporting, clinical trial safety, benefit-risk evaluation, and global regulatory safety compliance across pre-marketing and post-marketing products.
Professionals with expertise in signal detection, aggregate reporting, safety data analysis, and regulatory pharmacovigilance documentation are encouraged to apply.
Key Responsibilities
Establish and maintain the safety profile of products during development and post-marketing phases
Perform continuous safety surveillance using global safety data sources
Manage and contribute to safety governance committees throughout the product lifecycle
Present safety evaluations, risk-benefit analyses, and surveillance outcomes to internal stakeholders
Author and review pharmacovigilance regulatory documents including:
Development Safety Update Reports (DSURs)
Periodic Safety Update Reports (PSURs)
Serious Unexpected Suspected Adverse Reaction (SUSAR) reports
Risk Management Plans (RMPs)
Support Company Core Data Sheet (CCDS) updates and labeling maintenance activities
Provide medical and safety input for:
Clinical Trial Protocols
Clinical Study Reports
Investigator Brochures
Integrated Safety Summaries
Scientific Publications
Respond to Health Authority and Ethics Committee safety queries
Participate in Data Monitoring Committees and investigator training activities
Collaborate with global cross-functional teams in clinical safety and regulatory operations
Required Qualifications
MD or Master’s Degree in Medicine preferred
Strong experience in:
Signal Management
Aggregate Reporting
ICSR Management
Clinical Trial Safety
Pharmacovigilance Operations
Excellent understanding of global drug safety regulations and risk management processes
Proficiency in Microsoft Office tools including Word, Excel, PowerPoint, and Outlook
Strong analytical thinking, communication, and stakeholder management skills
Ability to work effectively in a fast-paced global healthcare environment
Preferred Candidate Profile
This opportunity is ideal for professionals currently working in:
Pharmacovigilance
Drug Safety Operations
Clinical Safety
Regulatory Safety
Aggregate Reporting
Signal Detection & Risk Management
Candidates with experience in global CROs, pharmaceutical companies, or life sciences organizations will be highly preferred.
About the Global Patient Safety Team
The Global Patient Safety division at Novo Nordisk in Bangalore plays a critical role in monitoring, evaluating, and communicating the safety profile of products across global markets. The team collaborates closely with international safety hubs and therapeutic experts focusing on Diabetes, Obesity, and Rare Disease portfolios.
The work environment is collaborative, innovation-driven, and highly focused on ensuring patient safety through scientific excellence and regulatory compliance.
Why Join Novo Nordisk?
Work with one of the world’s most respected pharmaceutical companies
Exposure to global pharmacovigilance and clinical safety operations
Opportunity to work on innovative therapies and chronic disease management programs
International collaboration with global healthcare experts
Strong professional growth and long-term career development opportunities
Application Deadline
Last Date to Apply: 25 April 2026
Important Recruitment Disclaimer
Novo Nordisk does not charge any fee during recruitment, training, or hiring processes. Applicants are advised to remain cautious of fraudulent job offers requesting payments, equipment purchases, or personal financial information.
How to Apply
Interested candidates can apply through the official Novo Nordisk careers portal. For more verified global Pharmacovigilance, Drug Safety, Clinical Research, Regulatory Affairs, and Healthcare jobs, visit ThePharmaDaily.com regularly.
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