Vertex UK Int'l HQ/R&D Posted October 26, 2026

Regulatory Strategy Senior Manager

Paddington, United Kingdom Full time
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Vertex UK Int'l HQ/R&D 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

Job Description

General Summary:

The Regulatory Strategy Senior Manager will be responsible for contributing regional or global regulatory strategy expertise for development programs or marketed products. The Regulatory Strategy Senior Manager will serve as a regional regulatory lead, or in some cases may also be a global regulatory lead, for development and/or commercial product(s) within the Vertex portfolio. This role requires understanding of regulatory affairs frameworks in the US, Europe, or other international markets, and understanding of drug development and related concepts.

Key Duties and Responsibilities: Leads the development and implementation of regulatory strategy for assigned region as a member of the global regulatory affairs functional team

Contributes to and may lead global regulatory strategy development for certain programs

Responsible for regulatory communications with local health authority; may independently lead regulatory interactions with the health authority

Provides guidance to teams on regulatory requirements for development and approval pathways for assigned region, including potential for expedited pathways

Manages the process for preparation, submission, and approval of regulatory applications within assigned region

Provides strategic and technical regulatory input for key product development or registration documents

Ensures compliance of regulatory submissions with current regulations and guidance

Reviews and evaluates regulatory intelligence and guidance information to continuously inform regulatory strategy in assigned region

Knowledge and Skills: In-depth knowledge of global and regional regulatory affairs frameworks

Good understanding of drug development and related concepts, such as clinical trial design, statistics, and clinical pharmacology

Good understanding of requirements and processes to maintain a product on the market; reporting and surveillance

Ability to assess and understand complex scientific information, regulatory precedent, competitive intelligence, and regulatory guidelines and make recommendations based on assessment

Strong problem-solving skills

Strong written and verbal communication skills to explain difficult information and build alignment

Ability to work effectively within a team environment

Ability to plan, prioritize, and execute work and projects in a systematic and efficient manner

Education and Experience: Bachelor's degree in Biology, Chemistry, or other related discipline

Typically requires 6 years of relevant pharmaceutical or biotech industry experience within regulatory affairs, or the equivalent combination of education and experience

At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.

Flex Designation:

Hybrid-Eligible Or On-Site Eligible

Flex Eligibility Status:

In this Hybrid-Eligible role, you can choose to be designated as:

1.    Hybrid: work remotely up to two days per week; or select

2.    On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Hybrid

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Paddington, 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 229 comparable Manager Regulatory Affairs roles across 70 biopharma companies.

229Comparable roles tracked
218Currently active
70Companies hiring similar roles
29Countries represented

Salary context

68 of 229 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Manager, Global Regulatory Strategy · Sarepta Therapeutics, Inc. $116,000/yr – $145,000/yr
Peer group range $130,500 – $236,300 (median $180,500)

Where these roles are based

Top locations among the 229 comparable roles

United States99
India27
United Kingdom19
Japan18
Ireland8
China7

+ 23 more countries

Seniority mix

229 of 229 peers have a known seniority level

Manager165
Associate Director52
Associate12

Therapeutic area mix

20 of 229 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology7
Oncology6
Ophthalmology4
Respiratory1
Rare Disease1
Dermatology & Aesthetics1

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.

60%similar
AbbVie Marlow, England Manager
Same function Same seniority Same country
60%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Same seniority Same country
60%similar
Ipsen Biopharm Ltd London (UK), United Kingdom Manager
Same function Same seniority Same country
60%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Same seniority Same country
60%similar
Regeneron UK Limited Uxbridge1, United Kingdom Manager
Same function Same seniority Same country
60%similar
Amgen Limited Cambridge, United Kingdom Manager
Same function Same seniority 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.

60%
Regulatory Affairs Manager Advertising and Promotion
AbbVie · Marlow, England · Manager
Function Therapeutic area Seniority Country
60%
Regulatory Submission Project Manager
Ipsen Biopharm Ltd · London (UK), United Kingdom · Manager
Function Therapeutic area Seniority Country
60%
Regulatory Affairs Senior Manager - UK and Ireland
Amgen Limited · Cambridge, United Kingdom · Manager
Function Therapeutic area Seniority Country
60%
Manager, Global Patient Safety Scientist
Regeneron UK Limited · Uxbridge1, 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.