Safety Surveillance Specialist – Pharmacovigilance
Category: Regulatory Affairs & Patient Safety / Pharmacovigilance
Location: Bangalore, Karnataka, India – Novo Nordisk Global Business Services (GBS)
Employment Type: Full-Time
Experience Required: Minimum 12 years in Pharmacovigilance / Patient Safety
Application Deadline: 31st January 2026
About the Role
Novo Nordisk is seeking an experienced Safety Surveillance Specialist to join our Global Patient Safety (GPS) team in Bangalore. This role is a critical part of our pharmacovigilance framework, responsible for ensuring patient safety, monitoring drug safety signals, and guiding benefit-risk assessments throughout the lifecycle of cardiometabolic products.
The ideal candidate will combine deep medical and scientific knowledge with regulatory expertise, analytical proficiency, and leadership in cross-functional teams to strengthen our safety strategy globally.
Key Responsibilities
Safety Surveillance & Signal Management: Conduct critical safety data analysis, detect safety signals, and evaluate potential risks to maintain an accurate and up-to-date product safety profile.
Risk Management & Benefit-Risk Assessment: Provide expert input on Risk Management Plans (RMPs), safety monitoring strategies, and regulatory safety reporting.
Clinical Support: Contribute to the design of clinical study protocols and safety monitoring plans, ensuring integration of safety data in study execution.
Regulatory Reporting & Documentation: Support product labeling, prepare regulatory submissions, and ensure accurate safety interpretations in compliance with global standards.
Cross-Functional Leadership: Build strong relationships across functions, mentor and coach team members, and provide strategic input in safety-related discussions with regulators, consultants, and partners.
Continuous Improvement: Support process improvements and contribute to long-term safety surveillance strategies.
Required Qualifications
Medical Degree (MBBS or MD) from an accredited institution.
Minimum 12 years of experience in pharmacovigilance, patient safety, or related fields, with proven delivery in signal management, RMPs, and aggregate reporting.
Strong understanding of drug development, regulatory frameworks, and global pharmacovigilance guidelines (ICH, GVP).
Experience in interpreting epidemiological data and applying integrative, evidence-based thinking for decision-making.
Excellent project management and stakeholder engagement skills; ability to operate in a matrix organization.
Strong analytical, leadership, and mentoring abilities; innovative mindset with contributions to long-term strategy.
Preferred Skills:
Experience in cardiometabolic therapeutic areas or related disease domains.
Demonstrated ability to influence safety strategy and drive initiatives across global teams.
About the Team
The Global Patient Safety – Safety Surveillance Adviser team at Novo Nordisk Bangalore monitors, evaluates, and communicates the safety profile of products throughout their lifecycle, focusing on Diabetes, Obesity, and Rare Disease portfolios. The team collaborates closely with global hubs in Denmark and other partner teams, ensuring a dynamic, collaborative, and fast-paced environment with a shared commitment to patient safety and positive benefit-risk outcomes.
Why Join Novo Nordisk
Contribute to a company with 100+ years of legacy in transforming patient health worldwide.
Work in a science-driven, inclusive environment where diverse perspectives and innovative ideas are valued.
Engage in meaningful career development, global collaboration, and leadership opportunities.
Play a central role in ensuring patient safety and shaping pharmacovigilance strategy globally.
Application Process
To apply, please submit your CV online via the “Apply” button.
Deadline: 31st January 2026
Disclaimer: Novo Nordisk does not charge fees for recruitment or request financial contributions. Be cautious of fraudulent job offers.
Summary:
This role is ideal for an experienced Medical Professional with 12+ years in Pharmacovigilance, specializing in signal detection, risk management, and patient safety surveillance, ready to lead global safety initiatives in a dynamic and innovative pharmaceutical environment.
Gujarat :
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