At a Glance
- Tasks: Lead global regulatory strategies for oncology, ensuring compliance and optimal approvals.
- Company: Join GSK, a global biopharma company with a mission to impact 2.5 billion lives.
- Benefits: Enjoy competitive salary, bonuses, healthcare, hybrid work, and career growth opportunities.
- Other info: Dynamic, inclusive culture focused on innovation and collaboration.
- Why this job: Make a real difference in patients' lives while working with cutting-edge science and technology.
- Qualifications: Bachelor's degree in biological or healthcare sciences; experience in regulatory affairs preferred.
The predicted salary is between 60000 - 80000 € per year.
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.
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. 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. We’re uniting science, technology, and talent to get ahead of disease together.
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.
In this role you will:
- 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.
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.
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 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.
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.
Manager, Global Regulatory Strategy, Oncology in London employer: Gsk
At GSK, we pride ourselves on fostering a culture where employees can thrive and feel valued, particularly in our London and Baar Onyx locations. With competitive salaries, comprehensive healthcare benefits, and a hybrid working model that promotes work-life balance, we empower our team to excel in their roles while contributing to our mission of improving global health. Our commitment to employee growth and innovation ensures that you will have the opportunity to develop your career in a supportive and dynamic environment focused on making a meaningful impact.
StudySmarter Expert Advice🤫
We think this is how you could land Manager, Global Regulatory Strategy, Oncology in London
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those at GSK. A friendly chat can open doors and give you insights that a job description just can't.
✨Tip Number 2
Prepare for interviews by practising common questions and scenarios related to regulatory strategy in oncology. We want to see your thought process and how you tackle challenges!
✨Tip Number 3
Show off your passion for patient care and innovation during interviews. GSK is all about making a positive impact, so let your enthusiasm shine through!
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, you’ll find all the info you need about life at GSK there.
We think you need these skills to ace Manager, Global Regulatory Strategy, Oncology in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Global Regulatory Strategy Manager. Highlight your experience in regulatory affairs and oncology, and don’t forget to showcase your strong communication skills!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Explain how your background aligns with GSK's mission and values. Be clear about your passion for patient care and how you can contribute to the team.
Showcase Collaboration Skills:Since this role involves working with cross-functional teams, emphasise your ability to collaborate effectively. Share examples of how you've successfully worked in matrix teams to achieve common goals.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the info you need about life at GSK there!
How to prepare for a job interview at Gsk
✨Know Your Oncology Stuff
Make sure you brush up on the latest trends and regulations in oncology. GSK is looking for someone who can navigate the complexities of drug development, so being well-versed in clinical trial requirements and licensing will give you a leg up.
✨Showcase Your Collaborative Spirit
Since this role involves working with cross-functional teams, be ready to share examples of how you've successfully collaborated in the past. Highlight your ability to foster a team environment and resolve challenges proactively.
✨Prepare for Regulatory Scenarios
Think about potential regulatory scenarios you might face in this role. Be prepared to discuss how you would approach developing and executing regulatory strategies while ensuring compliance with global and local requirements.
✨Communicate Clearly and Confidently
Strong communication skills are key for this position. Practice articulating your thoughts clearly and concisely, especially when discussing complex topics. This will help you make a strong impact during the interview.
