At a Glance
- Tasks: Lead global regulatory strategies for oncology, ensuring compliance and optimal approvals.
- Company: Join GSK, a leader in healthcare innovation with a focus on patient impact.
- Benefits: Enjoy competitive salary, bonuses, healthcare, hybrid work, and career growth opportunities.
- Other info: Dynamic hybrid work environment with a commitment to diversity and inclusion.
- Why this job: Make a real difference in patients' lives while working with cutting-edge technology.
- Qualifications: Bachelor’s degree in biological or healthcare science; 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.
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.
- 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.
- 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 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.
Manager, Global Regulatory Strategy, Oncology employer: GlaxoSmithKline
At GSK, we pride ourselves on fostering a culture where employees can thrive and feel valued. With competitive salaries, comprehensive healthcare benefits, and a hybrid working model, we empower our team members to achieve a healthy work-life balance while contributing to groundbreaking advancements in oncology. Our commitment to employee growth and inclusion makes GSK an exceptional place to build a meaningful career in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Manager, Global Regulatory Strategy, Oncology
✨Tip Number 1
Network like a pro! Reach out to people in the industry, especially those already at GSK. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for interviews by knowing your stuff! Research GSK’s recent projects in oncology and be ready to discuss how your experience aligns with their goals. Show them you’re not just another candidate, but someone who truly gets their mission.
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online platforms. The more comfortable you are talking about your skills and experiences, the better you’ll perform when it counts.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the team at GSK.
We think you need these skills to ace Manager, Global Regulatory Strategy, Oncology
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the role of Manager, Global Regulatory Strategy, Oncology. Highlight your relevant 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! Use it to explain how your background aligns with the job requirements. Be specific about your achievements and how they relate to the responsibilities outlined in the job description.
Showcase Your Collaborative Spirit:Since this role involves working with cross-functional teams, make sure to mention any experiences where you’ve successfully collaborated with others. We love seeing examples of teamwork and problem-solving in action!
Apply Through Our Website:We encourage you to apply through our website for a smooth application process. It’s the best way to ensure your application gets the attention it deserves. Don’t miss out on this opportunity!
How to prepare for a job interview at GlaxoSmithKline
✨Know Your Stuff
Make sure you brush up on the latest trends in oncology and regulatory affairs. Familiarise yourself with GSK's recent projects and how they align with global regulatory strategies. This will show that you're not just interested in the role, but also invested in the company's mission.
✨Showcase Your Collaboration Skills
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 collaborative environment and resolve challenges proactively, as these are key traits for success in this position.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past experiences where you had to navigate regulatory challenges or innovate under constraints. Prepare concise stories that demonstrate your strategic thinking and decision-making abilities.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready. Inquire about GSK's approach to regulatory strategy in oncology or how they measure success in this role. This not only shows your interest but also gives you valuable insights into the company culture and expectations.
