hirly

Vertex Pharmaceuticals

Regulatory Strategy Manager

Paddington, United Kingdom

See how you match this job — and similar ones. Free.

Upload your resume and hirly scores it against this role at Vertex Pharmaceuticals first, then against similar open jobs, and shows where you fit and why.

PDF or DOCX, up to 12MB. No sign-up to see your matches.

Get past the screening software and onto a recruiter's desk

hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.

  • Keywords matched to this posting
  • Fit score before you apply
  • Cover letter included
Tailor my resume for this job →

Apply from your AI assistant

Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.

Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.

hirly's read of this role

Seniority
Lead / management
Country
GB
Work mode
On-site / unstated
First seen by hirly
26 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

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

Original posting on Vertex Pharmaceuticals's site ↗

Listed on hirly, a job board. hirly is not the employer: Vertex Pharmaceuticals is hiring for this role.

Browse similar roles

Want this one?

Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.

Tailor my resume for this job