Global Regulatory Affairs Manager

Global Regulatory Affairs Manager

Closing Date: 3rd September 2026 (COB)

Business Introduction
At GSK we have bold ambitions for patients aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform peoples lives. GSK fosters a culture ambitious for patients accountable for impact and committed to doing the right thing making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success. Were uniting science technology and talent to get ahead of disease together.
Find out more:
Our approach to R&D

For candidates seeking to be located at our Stevenage site this role will temporarily be based at Stevenage. However the Company plans to relocate its offices to Cambridge UK. The location of this role will therefore subsequently change to Cambridge UK in accordance with timelines to be set by the Company. The relocation is currently proposed to take effect by early 2029.

Position Summary
As a Global Regulatory Affairs Manager at GSK you will develop and execute global and regional regulatory strategies for oncology assets ensuring optimal labeling and approvals while maintaining compliance with internal and external requirements. You will be accountable to the Global Regulatory Lead (GRL) and Global Regulatory Therapeutic Area (TA) Head and collaborate with cross-functional teams to shape development plans and regulatory interactions across multiple regions. We value clear thinking collaboration practical problem solving and a patient-first mindset.

Responsibilities
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

• Work closely with GRL global/regional counterparts and local operating companies to develop and deliver robust regulatory strategies that meet key market requirements.

• Collaborate with cross-functional teams to align regulatory plans withMedicines Development Strategy and Integrated Asset Plan.

• Support interactions reviews and submissions with regional/local regulatory authorities for product development and approval.

• Assess regulatory intelligence precedents and competitive landscape to inform strategy development and improve decision-making.

• Ensure compliance with global regional and local regulatory requirements throughout the product lifecycle.

• Drive process improvement innovation and performance excellence through the development and implementation of strategic changes.

Location and Working Pattern

This role is based in GSK HQ in London UK Stevenage UK or alternatively in Switzerland Baar Onyx. The working pattern is hybrid combining time in the office and remote work.

Basic Qualification
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:

• Minimum: Bachelors degree in biological pharmaceutical or healthcare science.

• Proven experience in drug development process preferably in regulatory affairs and oncology.

• Knowledge of clinical trial and licensing requirements in at least one major regional/global market.

• Strong written and verbal communication skills for clarity and impact.

• Experience working effectively in matrix teams.

Preferred Qualification
If you have the following characteristics it would be a plus:

• Advanced scientific degree (PhD MD PharmD).

• Proven ability in managing global andregional development submission and approval activities.

• Demonstrated ability to foster collaborative environments proactively resolve challenges and develop innovative solutions within regulatory constraints.

• Proficiency in digital fluency tools to enhance project delivery efficiency and innovation.

Ready to apply
If this role feels like the right next step we encourage you to apply. Please submit your CV and a brief cover letter outlining how your experience matches the role. We look forward to hearing from you.

Skills

Why GSK

Uniting science technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade as a successful growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory immunology and inflammation; oncology; HIV; and infectious diseases to impact health at scale.

People and patients around the world count on the medicines and vaccines we make so were committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients accountable for impact and doing the right thing is the foundation for how together we deliver for patients shareholders and our people.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.

We believe in an agile working culture for all our roles. If flexibility is important to you we encourage you to explore with our hiring team what the opportunities are.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at where you can also request a call.

Please note should your enquiry not relate to adjustments we will not be able to support you through these channels. However we have created a Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSKs commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license GSK may be required to capture and report expenses GSK incurs on your behalf in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSKs compliance to all federal and state US Transparency requirements. For more information please visit the Centers for Medicare and Medicaid Services (CMS) website at Experience:

Manager