Novo Nordisk Posted August 10, 2026

Safety Surveillance Adviser I (Bangalore, Karnataka, IN)

Bangalore, India Type not listed
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Novo Nordisk is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Company: Novo Nordisk Global Business Services (GBS)

Shape the safety profile of medicines that reach millions of patients worldwide – from first-in-human trials through to marketed products across diabetes, obesity, and rare diseases.

Your new role

As a Safety Surveillance Adviser in Global Patient Safety (GPS), you will be at the centre of product safety – establishing safety profiles during development, maintaining labelling for marketed products, and conducting ongoing surveillance of Novo Nordisk products across their entire lifecycle.

Your key responsibilities will include:

Acting as Owner of the safety sections of labelling for the evolving Company Core Data Sheet (CCDS) for development products, maintaining labelling for marketed products, and providing safety input as a labelling change request (LCR) reviewer

Preparing relevant sections of Development Safety Update Reports (DSURs), periodic SUSAR reports, Periodic Safety Update Reports (PSURs), and clinical Risk Management Plans (RMPs) according to implementation plans or as required by Health Authorities

Establishing, operating, and chairing the Novo Nordisk cross-functional safety committee throughout the product lifecycle – presenting analysis and results of ongoing safety surveillance at pre-defined intervals for endorsements and recommendations

Providing safety input to Product Development Plans, Trial Outlines, Protocols, Clinical Trial Reports, Investigator's Brochures, integrated safety summaries, abstracts, and planned publications

Responding to enquiries from Health Authorities and Ethics Committees regarding safety aspects of protocols and Patient Information/Informed Consent, and ensuring deliverables to and from Data Monitoring Committees

Delivering proactive safety communication through participation in project and trial teams, and conducting Investigator training as required

Your new department

In Research & Development, you'll be part of a unit that explores bold scientific ideas and advances them into clinical testing. We combine curiosity, AI tools, and human data to develop transformative therapies. Through collaboration and operational excellence, we shape and deliver an innovative pipeline to meet future patient needs.

The Safety Surveillance Adviser team at Global Patient Safety (GPS) is based in Bangalore, India, and collaborates closely with global hubs in Søborg, Denmark, and other partner teams. The team is responsible for monitoring, evaluating, and communicating the safety profile of Novo Nordisk products across their lifecycle – covering therapeutic portfolios in Diabetes, Obesity, and Rare Diseases. The atmosphere is dynamic, collaborative, and fast-paced, with a shared mission to ensure patient safety and maintain a favourable benefit-risk balance.

Your skills & qualifications

We're looking for a Safety Surveillance Adviser who thrives in a fast-paced environment and is passionate about patient safety. You'll bring with you:

A Master's degree in Medicine/MD post MBBS (preferred)

Relevant experience in Signal Management, Aggregate Management, and Individual Case Safety Report (ICSR) handling

Ability and willingness to quickly adjust to changes in a continuously developing environment

Comfortable use of the Microsoft Office package (Outlook, Word, Excel, and PowerPoint)

Strong communication skills and fluency in English, with the ability to convey complex safety information clearly to diverse stakeholders

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Job details

Seniority
Not listed
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Bangalore, India
Employment type
Not listed

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 160 comparable Pharmacovigilance roles across 54 biopharma companies.

160Comparable roles tracked
145Currently active
54Companies hiring similar roles
32Countries represented

Salary context

33 of 160 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Safety Project Manager · IQVIA $86,000/yr – $214,800/yr
Peer group range $150,400 – $380,650 (median $264,000)

Where these roles are based

Top locations among the 160 comparable roles

United States65
China14
Japan8
France8
India8
United Kingdom8

+ 26 more countries

Seniority mix

113 of 160 peers have a known seniority level

Director33
Senior24
Manager24
Intern/Fellow/Postdoc9
Associate Director7
Associate6
Senior Director5
Principal4
Executive/VP1

Therapeutic area mix

24 of 160 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology11
Neuroscience6
Immunology3
Vaccines & Infectious Disease1
Ophthalmology1
Respiratory1
Rare Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Manager
Same function Same country
40%similar
Amgen Technology Pvt Ltd. Hyderabad, India Senior
Same function Same country
40%similar
AstraZeneca Bangalore, India Director
Same function Same country
40%similar
Novo Nordisk Bangalore, India
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Pharmacovigilance job in India, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Senior Manager - Regulatory Data Management
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Pharmacovigilance Operations Manager
Amgen Technology Pvt Ltd. · Hyderabad, India · Manager
Function Therapeutic area Seniority Country
40%
Jr Assoc Pharmocovigilance (Bangalore, Karnataka, IN)
Novo Nordisk · Bangalore, India · Seniority not listed
Function Therapeutic area Seniority Country
25%
Director, Patient Safety (MD)
Gilead Sciences, Inc. · Foster City, United States · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.