Assessment Centre Date: January - February 2025
Are you a talented and driven student or graduate eager to make an impact on billions of lives? Apply for the Global Clinical Delivery Graduate programme at GSK today!
GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.
Our success absolutely depends on our people. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get ahead together.
With over 300 years of innovation, we’re a science-led global healthcare company that discovers, develops and manufactures innovative medicines and vaccines. Join us and help millions of people do more, feel better, live longer.
Are you ready to use your skills to deliver high quality clinical trials?
If so, you could be suited to this role! Together we can design, plan and deliver clinical trials across a range of therapeutic areas, delivering medicines and vaccines to our patients.
Ahead together with tailored training and career development
- We’ll tailor your training and development to suit your talents and ambition, as well as our business needs, setting you up for success in your chosen niche. The skills you learn on our Graduate programme can be used across many areas of our business and, potentially, many countries. There’s no limit to how far you can go with us – it’s up to you to prove yourself.
- Over the next two years, the Graduate Programme will challenge and support you to grow both professionally and personally. You will have fascinating rotations to explore study management for Research (Rx) and Vaccines (Vx) projects and the landing role will be in Global Clinical Delivery team.
- If you are a graduate with the passion to take accountability for designing, planning and executing the delivery of global Phase I to IV clinical trials to ensure it is delivered on time, to a high quality, within budget and all in line with company standards and scientific requirements, then this is a role for you!
- You will have the opportunity to operate as a Study Manager (SM) and contribute to deliver the clinical study to time, cost and quality, ensuring inspection readiness by taking an oversight over project conduction. You will have a broader impact on the business, by driving continuous improvement initiatives within their remit of expertise, sharing best practices across business, with a focus on increasing operational delivery efficiency. You will also build close collaborations with other SMs, Study Delivery Leads (SDLs) and Study Delivery Specialists (SDSs) to share best practices, experience and support process improvement.
- On completion, you will have had the opportunity to develop key skills in study management along with gaining experience of working with functional subject matter experts to help you succeed as a SM.
What will you do?
- Manage study execution of trial(s) from start-up through close-out in accordance with study budget and timelines with the focus on setting up, maintaining and ensuring completeness of internal systems/databases/tracking tools and project plans
- Work in collaboration with the SDL to provide end to end operational and administrative support for study delivery activities
- Monitor study conduct and progress, identify, resolve and escalate risks/issues which may impact delivery of the study to the necessary quality, timeline and budget objectives
- Interact with other study team members across different functions to ensure all issues, risks and successes with study delivery are reviewed and/or shared as they occur
- Support Clinical Team in quality and data oversight to ensure inspection/audit readiness, including oversight of eTMF completeness
- Facilitate and maintain interactions and meetings with internal and external vendors to ensure the successful delivery of assigned studies.
- Set up and maintenance of clinical trial management systems and tracking tools
- Prepare and update of study documents and study plans
- Learn about the drug development process
- Gain broad experience across the field of clinical research and variety of therapeutic areas
- Learn to manage projects and prioritise tasks