Novo Nordisk – Safety Surveillance Adviser | Bangalore, India | Pharmacovigilance
Company: Novo Nordisk
Location: Bangalore, Karnataka, India
Job Type: Full-Time
Work Mode: On-site
Experience: Mid-Level (Pharmacovigilance / Drug Safety)
Qualification: MD / Master’s in Medicine or Life Sciences (Preferred)
Compensation: Not disclosed in the job description
Application Deadline: April 8, 2026
Pharmacovigilance and drug safety jobs in India are among the fastest-growing pharma career paths, and this role offers deep exposure to global safety surveillance, signal detection, and regulatory safety reporting.
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Job Summary
Novo Nordisk is hiring a Safety Surveillance Adviser to support global pharmacovigilance operations and ensure the safety profile of products across clinical development and post-marketing phases. This role is critical in maintaining drug safety, benefit-risk balance, and regulatory compliance through continuous safety monitoring and reporting.
You will work within the Global Patient Safety (GPS) team, contributing to signal management, aggregate reporting, risk management plans, and regulatory safety submissions while collaborating with global stakeholders.
This is an ideal role for professionals aiming to build expertise in:
Pharmacovigilance (PV)
Drug Safety & Risk Management
Regulatory Affairs & Safety Reporting
Clinical Trial Safety
Key Responsibilities
Safety Surveillance & Signal Management
Perform ongoing safety surveillance for products in pre-approval and post-marketing phases
Identify, evaluate, and communicate safety signals from global data sources
Maintain product safety profiles and ensure benefit-risk balance
Aggregate Reporting & Regulatory Compliance
Author and review key pharmacovigilance documents:
Development Safety Update Reports (DSURs)
Periodic Safety Update Reports (PSURs)
SUSAR reports
Risk Management Plans (RMPs)
Respond to queries from Health Authorities (HAs) and internal stakeholders
Labeling & Safety Documentation
Own and maintain safety sections of:
Company Core Data Sheet (CCDS)
Product labeling for marketed drugs
Provide safety input for labeling change requests (LCRs)
Clinical Trial Safety & Risk Management
Provide safety input into:
Clinical Trial Protocols
Investigator’s Brochures (IB)
Clinical Study Reports (CSR)
Support Data Monitoring Committees (DMCs) and Ethics Committees (ECs)
Cross-Functional Collaboration
Chair and manage cross-functional safety committees
Collaborate with clinical development, regulatory, and medical teams
Conduct investigator training and safety communication sessions
Required Skills & Qualifications
MD (preferred) or Master’s degree in Medicine, Pharmacy, Life Sciences, or related field
Experience in:
Signal Management
Aggregate Reporting (DSUR, PSUR)
Individual Case Safety Reports (ICSRs)
Strong knowledge of:
Pharmacovigilance systems and processes
Global drug safety regulations
Clinical trial safety requirements
Familiarity with:
ICH-GVP guidelines
Risk Management Plans (RMPs)
Safety databases and reporting tools
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
Strong analytical, communication, and stakeholder management skills
Perks & Benefits
Work with a global leader in diabetes, obesity, and rare disease therapeutics
Exposure to international pharmacovigilance and regulatory frameworks
Opportunity to lead safety committees and global safety strategies
Collaborative and high-impact work environment
Career growth in drug safety, regulatory affairs, and clinical development
About the Company
Novo Nordisk is a global healthcare leader with over 100 years of expertise in diabetes care, obesity management, and rare diseases. The company is known for its strong focus on patient safety, innovative therapies, and sustainable healthcare solutions.
Why This Role is High-Value in Pharma Careers
The Safety Surveillance Adviser role sits at the core of modern drug development. With increasing regulatory scrutiny and patient safety requirements, pharmacovigilance professionals are in high demand globally.
This role provides direct exposure to:
Global safety reporting systems
Regulatory submissions to health authorities
Clinical trial safety oversight
Risk-benefit analysis of pharmaceutical products
This makes it a powerful career move toward roles like:
Drug Safety Physician
Pharmacovigilance Scientist
Risk Management Specialist
Regulatory Safety Lead
Application Process
Apply through the official Novo Nordisk careers portal
Upload updated CV highlighting pharmacovigilance and safety experience
Ensure alignment with key keywords like:
Pharmacovigilance
Signal Detection
ICSR Processing
DSUR / PSUR
Risk Management Plans
Call to Action
If you want to build a career in pharmacovigilance, drug safety, and global regulatory affairs, this is your chance to work on high-impact therapies that improve millions of lives.
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