Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Safety Surveillance Specialist

Novo Nordisk
Novo Nordisk
12+ years
preferred by company
10 Jan. 30, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Safety Surveillance Specialist

Category: Regulatory Affairs & Pharmacovigilance
Department: Global Patient Safety
Location: Bengaluru, Karnataka, India
Work Location: Novo Nordisk Global Business Services (GBS), India
Job Type: Full-Time
Experience Required: 12+ years
Application Deadline: 31 January 2026


Job Overview

Novo Nordisk is seeking a highly experienced Safety Surveillance Specialist to join its Global Patient Safety team in Bengaluru. This senior-level role is responsible for leading safety surveillance strategy and execution across the entire product lifecycle, with a strong focus on cardiometabolic therapeutic areas.

The position offers the opportunity to play a critical role in evaluating product safety, driving signal management, supporting regulatory decision-making, and ensuring a robust benefit–risk profile for innovative therapies that address serious chronic diseases.


Key Responsibilities

  • Establish, maintain, and communicate the product safety profile through advanced safety data analysis and interpretation.

  • Lead pharmacovigilance and safety surveillance planning, developing and executing lifecycle safety strategies.

  • Perform signal detection, validation, and evaluation, including expert review of safety data and scientific literature.

  • Provide authoritative input into benefit–risk assessments and contribute to global Risk Management Plans (RMPs).

  • Support clinical study design by defining safety monitoring strategies within clinical protocols.

  • Develop and maintain Core Reference Safety Information (CRSI) and support global product labeling activities.

  • Ensure accurate safety conclusions are documented within regulatory submissions and aggregate safety reports.

  • Participate in and contribute to global safety governance forums and committees.

  • Represent Safety Surveillance in discussions with regulatory authorities, external partners, and consultants.

  • Build strong cross-functional relationships and demonstrate leadership within a global matrix organization.

  • Mentor and coach team members, supporting capability building and long-term safety strategy development.


Qualifications & Experience

  • Medical Degree (MBBS or MD) from a recognized and accredited institution.

  • Minimum 12 years of progressive experience in pharmacovigilance, patient safety, or safety surveillance roles.

  • Extensive hands-on experience in signal management, aggregate safety reporting, and Risk Management Plans (RMPs).

  • Strong knowledge of global drug development processes and regulatory frameworks.

  • Proven ability to interpret epidemiological and real-world safety data using an integrated, scientific approach.

  • Demonstrated expertise in project and stakeholder management within global environments.

  • Strategic mindset with a track record of driving process improvements and long-term safety initiatives.

  • Excellent communication, analytical, and leadership skills with a strong focus on quality and compliance.


About the Global Patient Safety Department

The Safety Surveillance Adviser team within Global Patient Safety (GPS) is based in Bengaluru and plays a vital role in monitoring, evaluating, and communicating the safety profiles of Novo Nordisk products across their full lifecycle. The team supports global therapeutic portfolios in Diabetes, Obesity, and Rare Diseases, working closely with international hubs in Søborg, Denmark, and other global partner teams. The work environment is collaborative, fast-paced, and driven by a shared commitment to patient safety and scientific excellence.


Working at Novo Nordisk

Novo Nordisk is a global healthcare company with more than a century of innovation focused on defeating serious chronic diseases. The organization is driven by scientific curiosity, long-term thinking, and a strong commitment to improving patient lives worldwide. Employees are empowered to contribute beyond their roles, collaborate across borders, and create sustainable healthcare solutions with lasting impact.

Novo Nordisk is committed to diversity, inclusion, and equal opportunity, ensuring a fair and transparent recruitment process for all candidates.


Recruitment Disclaimer

Novo Nordisk does not extend unsolicited employment offers and does not charge fees at any stage of the recruitment process. All legitimate communications originate from official Novo Nordisk channels. Candidates are advised to remain vigilant against fraudulent job offers.


SEO & Search Optimization Keywords

Safety Surveillance Specialist jobs in Bengaluru, Pharmacovigilance jobs India, Global Patient Safety careers, Signal Management roles, Risk Management Plan jobs, Novo Nordisk safety jobs, Regulatory Affairs and PV careers.