Pfizer R&D UK Limited Posted October 13, 2026

Undergraduate Regulatory Strategist

Walton Oaks, United Kingdom Full time
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Pfizer R&D UK Limited 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

  ­­ Pfizer UK Undergraduate Programme 2027-2028

Undergraduate Regulatory Strategist

Global Regulatory Sciences

Regulatory Strategy

Department Overview

·         Regulatory Strategy is a dynamic department which proactively collaborates with drug development and various functional lines to ensure Pfizer meets the requirements of Global Health Authorities.

·         Working across all stages of the pharmaceutical product life cycle, Regulatory Strategists aim to secure regulatory approval in a compliant, creative, efficient and commercially viable manner by defining and executing asset-specific regulatory strategies.

·         The Regulatory Strategy department leads dialogue with Global Health Authorities on behalf of Pfizer.

·         Regulatory Strategy engages with different business functions and regions, offering unique insight to research & development and commercial aspects of the pharmaceutical industry.

What can I achieve and what will I be responsible for whilst completing a placement at Pfizer?

 

Global Regulatory Sciences supports a diverse portfolio of products spanning multiple therapeutic areas (Inflammation and Immunology & Non-malignant haematology, Internal Medicine, Vaccines, Global Brands). You will have the opportunity to develop and implement regulatory strategies for innovative medicinal products and to maintain Pfizer’s marketed products to the highest standards of quality, safety and efficacy, across different regions. Products can be at any stage in the pharmaceutical product life cycle (pre-approval or post-approval) and so you will have a unique overview of the company, seeing therapies from research stages, through clinical development and onto the market.

You will be a part of the day-to-day compilation of general regulatory project documents, clinical trial applications, regulatory dossiers and responses to regulatory questions received from health authorities. You will also contribute to global regulatory strategies and implementation plans, ensuring an aligned regional position is reached and agreed for assigned projects. You will monitor progress of regulatory plans whilst ensuring identified risks are addressed. Moreover, you will take a proactive role in maintaining systems, processes and procedures relating to regulatory strategy.

 

What other opportunities and benefits do Pfizer offer?

 

Pfizer has consistently ranked amongst the top 100 graduate employers globally and offers many additional opportunities in the form of:

·         Communication and presentation training

·         Volunteering opportunities

·         Participation in cross-functional projects

·         Shadowing opportunities

·         Professional membership for The Organization for Professionals in Regulatory Affairs (TOPRA)

·         Opportunity to attend UK-based TOPRA Careers Fair

·         Flexible working arrangements

·         Pfizer Share Ownership Plan

When can I start?

 

Placements will start on the 1st September 2027 and will run for 12 months.

 

PERSON SPECIFICATION

 

Type of person we are looking for, in relation to ‘Skills’, ‘Knowledge’ and ‘Motivation’:

 

·         Completing placement as part of University Degree either through Year In Industry/Industrial Placement or Gap Year

·         Adaptable – Desire to learn and a capacity to assimilate and act on new information quickly

·         Analytical –Synthesize complex information and identify potential issues before they arise

·         Integrity & Attention to Detail – Appreciate the core function of Regulatory Strategy and work to provide the best outcomes for patients.

·         Problem-solving – Use innovative and strategic thinking to develop novel solutions to challenges

·         Project management – Ability to manage multiple activities and complete tasks on time.

·         Proactive – Self-starter with the ability to work individually and as a team.

·         Written & Oral Communication – Ability to convert complex data into succinct messages

·         IT Expertise - Proficient in the use of Microsoft Office suite of programmes

·         AI Literate

Who can apply?

Applicants must be completing placement as part of a life science degree course at a UK University, either through Year in Industry/Industrial Placement or Gap Year.

 

This position will close for applications on 1st November 2026.

Please note that we only accept application forms. Please do not send over your CV or cover letter as they will not be considered.

Please access the Word version of the Application Form here: Undergraduate Vacancies | Pfizer UK and find instructions as to how to complete your application and more about eligibility criteria.

#LI-PFE

Work Location Assignment: Hybrid

Purpose

Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.

Digital Transformation Strategy

One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.

Flexibility

We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let’s start the conversation!

Equal Employment Opportunity

We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.

DisAbility Confident

We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on  Pfizer Careers .

Support Services

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Walton Oaks, United Kingdom
Employment type
Full time

How this role compares

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

We currently track 554 comparable Regulatory Affairs roles across 107 biopharma companies.

554Comparable roles tracked
532Currently active
107Companies hiring similar roles
49Countries represented

Salary context

152 of 554 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
Highest disclosed · Executive Director, Medical Writing · Regeneron Pharmaceuticals, Inc (USA) $285,600/yr – $475,900/yr
Peer group range $75,038 – $380,750 (median $198,225)

Where these roles are based

Top locations among the 554 comparable roles

United States231
India44
Japan33
United Kingdom30
Poland25
Ireland21

+ 43 more countries

Seniority mix

432 of 554 peers have a known seniority level

Manager181
Director73
Associate Director53
Senior46
Senior Director22
Intern/Fellow/Postdoc22
Principal15
Associate10
Executive/VP10

Therapeutic area mix

44 of 554 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology14
Immunology10
Rare Disease6
Dermatology & Aesthetics5
Neuroscience3
Vaccines & Infectious Disease3
Cardiovascular / CVRM2
Respiratory1

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
AbbVie Maidenhead, ENGLAND Manager
Same function Same country
40%similar
Vertex UK Int'l HQ/R&D Paddington, United Kingdom Director
Same function Same country
40%similar
AbbVie Marlow, England Manager
Same function Same country
40%similar
Ipsen Biopharm Ltd London (UK), United Kingdom Director
Same function Same country
40%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Same country
40%similar
Regeneron UK Limited Uxbridge1, United Kingdom Director
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 Regulatory Affairs job in the United Kingdom, 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 Affairs
AbbVie · Maidenhead, ENGLAND · Manager
Function Therapeutic area Seniority Country
40%
Regulatory Affairs Manager Advertising and Promotion
AbbVie · Marlow, England · Manager
Function Therapeutic area Seniority Country
40%
EU Regulatory Affairs Manager (Biosimilars)
Amgen Limited · Uxbridge, United Kingdom · Manager
Function Therapeutic area Seniority Country
40%
Senior Regulatory Submission Project Manager
Ipsen Biopharm Ltd · London (UK), United Kingdom · Manager
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.