We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
We embrace modern work practices; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in‑office work.
Manager, Global Regulatory Strategy, Oncology – London, UK or Baar Onyx, Switzerland
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 people’s lives.
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.
Responsibilities
- 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 with Medicines 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.
Basic Qualifications & Skills
- Minimum: Bachelor’s degree in a biological, pharmaceutical or healthcare science.
- 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 Qualifications & Skills
- Advanced scientific degree (PhD, MD, PharmD).
- Proven ability in managing global and regional 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.
Location and Working Pattern
This role is based in London, United Kingdom or Baar Onyx, Switzerland. The working pattern is hybrid, combining time in the office and remote work.
How to apply
If this role speaks to you and you meet the basic qualifications, we would love to hear from you. Please submit your CV and a short cover letter that explains how your experience aligns with the role. Apply now to take the next step in your regulatory career.
Application close date – 2nd June 2026, COB.
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.
To request adjustments to our application process to assist you in demonstrating your strengths and capabilities, please contact: UKRecruitment.Adjustments@gsk.com.
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