Novo Nordisk Posted September 26, 2026

Pharmacovigilance Specialist (Dubai, Dubai, AE)

Dubai, United Arab Emirates 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

Location: Dubai, United Arab Emirates

Your work will directly safeguard patients by ensuring the safety of medicines that millions of people depend on every day. In this role, you will be at the intersection of science, regulation and patient care – playing a critical part in how Novo monitors, evaluates and acts on safety data across our growing portfolio.

Your new role

As a Pharmacovigilance Specialist based in the UAE, you will be responsible for ensuring that safety information about Novo Nordisk products is collected, assessed and reported in compliance with local and global regulatory requirements. You will work in a dynamic environment where the portfolio is expanding rapidly, and your expertise directly protects patients.

Your key responsibilities will include:

Acting as the QPPV for Novo products in UAE.

Maintenance of the PV system within the affiliate in accordance with internal SOPs and local regulations.

Reporting of ADRs to Global Safety & UAE EDE within set timelines.

Handling technical complaints.

Periodic training of NN UAE employees on the handling of safety information.

Provision of PV onboarding training to external vendors, such as those involved with PSPs and MRPs.

Managing Safety Data exchange Agreements with partners.

Timely submission of PSURs and RMPs to local authority.

Daily check and review of the local PV Safety Mailbox

Local requirements process is executed timely and effectively

As a person, you thrive in diverse environments where collaboration is key to success. You are adaptable and able to manage complex tasks in a changing environment while maintaining patient focus and the highest level of integrity.

Your new department

MRPV department is including medical affairs function responsible of all medical activities in the affiliate and the Regulatory Affairs & Pharmacovigilance functions responsible for all the regulatory activities related to the registration of pharmaceutical products and medical devices, keeping their life cycle management and the reporting the customer complaints, adverse events and submission of Periodic Safety Update Reports (PSURs) and Risk Management Plan (RMPs) to the local authority.

Your skills & qualifications

To be successful in this role, you should have the following:

A Bachelor’s degree in pharmacy (essential)

A minimum of 3 years of experience in Pharmacovigilance

Fluency in written and spoken English and Arabic

Has knowledge of local/global pharmacovigilance regulations.

Sound understanding and experience of Pharmacovigilance Agreement lifecycles

High level of computer literacy, including MS Office

Good attention to detail and problem-solving ability

Excellent communication skills and ability to engage effectively with all levels within the organisation; strong collaborator with proven customer and stakeholder management skills

Ability to independently prioritise and manage workload to meet deadlines

Ability to work as part of a team as well as autonomously

Ability to manage operational PV tasks while contributing to the business strategy

Ability to review and simplify operational activities to find efficiencies

Working at Novo

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.

Salary: The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience. Further details to be shared during the recruitment process.

Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

Learn more about our Reward Philosophy  here

Deadline

Apply before 7 October. Applications are reviewed on an ongoing basis. To submit your application, please upload your CV and motivational letter online (click on Apply and follow the instructions). Internal candidates are kindly requested to inform their line managers before applying.

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

At Novo, 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.

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Job details

Seniority
Not listed
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Dubai, United Arab Emirates
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 112 comparable Pharmacovigilance roles across 40 biopharma companies.

112Comparable roles tracked
108Currently active
40Companies hiring similar roles
22Countries represented

Salary context

33 of 112 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 · Technical Assistant, PV Operations · Mylan Pharmaceuticals Inc. $37,000/yr – $73,000/yr
Peer group range $55,000 – $429,500 (median $264,000)

Where these roles are based

Top locations among the 112 comparable roles

United States49
India11
Japan8
France8
Germany7
United Kingdom6

+ 16 more countries

Seniority mix

84 of 112 peers have a known seniority level

Director23
Senior20
Manager20
Associate Director7
Intern/Fellow/Postdoc5
Associate4
Senior Director3
Principal2

Therapeutic area mix

18 of 112 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology7
Immunology4
Neuroscience3
Rare Disease2
Ophthalmology2

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.

25%similar
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25%similar
Gilead Sciences, Inc. Foster City, United States Director
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25%similar
Mylan AB Solna, Sweden Manager
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Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Celgene - Summit (Corp) Princeton, United States Senior Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Director
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Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
BMS Services Sp. z o.o. Warsaw, Poland Associate
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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.

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.

25%
Medical Director, Neuroscience, Global Patient Safety
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
25%
Senior Director, Medical Safety Assessment Program Lead, Neuroscience
Celgene - Summit (Corp) · Princeton, United States · Senior Director
Function Therapeutic area Seniority Country
25%
Senior Pharmacovigilance Associate
BMS Services Sp. z o.o. · Warsaw, Poland · Senior
Function Therapeutic area Seniority Country
25%
Global Periodic Reporting Lead
Genzyme Corporation · Cambridge, United States · Seniority not listed
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.