Regulatory Affairs Graduate Programme, UK, 2027

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About the role

Join the GSK Regulatory Affairs Graduate Programme, UK, 2027:  Help us get ahead of disease together Important Application Update:   We have received a high volume of applications for this opportunity. The role will close for applications at 12:00pm UK time on Friday 2 October 2026.  Candidates wishing to be considered must submit their application before the closing time. Education required: Bachelor's degree from an accredited college/university, in a life science disciplines. Graduation by September 2027F Language requirement: Written and spoken fluency in English Other requirements:   Willingness to be geographically mobile (domestic) throughout rotations Location: GSK HQ, London Start date: September 2027 Application Information : *You can apply to only one GSK Graduate Programme in UK, so you can focus on the role that motivates you the most. Application deadline: A pplications are reviewed on a rolling basis, and this role will close once we have received enough applications. We recommend you apply as soon as possible. Assessment Centre Date: November/December See what our graduate programme participants have to say about their experiences in our GSK Graduate Programmes https://www.youtube.com/watch?v=-ybQQr9HKg8 ! Are you a talented, driven student or graduate eager to make an impact on billions of lives? Join the Regulatory Affairs Graduate Programme at GSK and get ahead with tailored training and career development designed to help you grow. Are you an analytical graduate who can help us ensure our medicines meet rigorous legal standards? This will be your challenge within our dedicated regulatory affairs department. It is here that we advise on legal and scientific requirements; collect, collate, and evaluate scientific data in order to confirm the quality and efficacy of our products – and keep track of changing global health authority requirements. We are required to meet stringent standards as part of the registration for clinical trials and marketing approvals across the world. You can be instrumental in this crucial process. Working with different areas of the function, other departments and colleagues from around the world, you will get an unparalleled insight into a critical team and the chance to provide expert guidance. If you’re a graduate with the talent and ambition to lead others, we’ll help you develop the expertise to become one of our GSK graduates. Over two years, our graduate programme will challenge and support you to grow professionally and personally. You will have stretching rotations supporting areas such as Global Regulatory Operations (GRO), Chemistry, Manufacturing and Controls (CMC), and/or the UK and Ireland business. As you experience these varied fields of expertise, you will learn exactly what it takes to get a drug approved.   With access to first-class support and development opportunities, you will be well-equipped to start your professional career and make a meaningful impact at GSK.   What will you do? • The timely provision of documentation to agreed timeframes for assigned projects. This may include, but is not limited to, support for clinical trials, marketing applications or activities relating to licence maintenance worldwide. The preparation, review and delivery of day-to-day submissions. • Manage workload and prioritise tasks to meet agreed deadlines, as outlined by the line manager, and handle multiple assignments simultaneously • Develop knowledge of the drug development process, regulatory agency guidelines, regulatory expectations and the principles of the regulatory review processes in Europe, Emerging Markets, Asia Pacific and North America. • Seek to resolve problems in a proactive manner, discussing problems with line manager to obtain advice and endorsement

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