Supported Studies Asset Study Delivery Lead - 14 month secondment/FTC in London

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.

The Asset Study Delivery Lead works in partnership with the Therapeutic Area Accountable Person (TA AP) and Supported Studies Operations Director to manage the end-to-end portfolio delivery of TA aligned studies. Accountable for providing end to end Supported Study (SS) portfolio delivery leadership at an Asset level. The Asset Study Delivery Lead will coordinate the review and outcome dissemination for Investigator Initiated Sponsored (IIS) and Supported Collaborative Studies (SCS) proposals for the TA. Responsible for the delivery of the Asset’s study portfolio, including milestone and budget forecast and management, prioritisation of studies and leading communication with key stakeholders. The Asset Study Delivery Lead may be responsible for one or more assets and will also have Study Delivery Lead (SDL) responsibilities.

In this role you will:

• Lead the coordination of proposal submissions and facilitation of the proposal review with matrix key stakeholders including LOC, safety, supply, legal, medical affairs, stats and external investigators, as per standard procedures.
• Communicate the proposal review outcome to external and internal stakeholders.
• Ensure IdeaPoint and Veeva are updated with the documentation and information from submission up to proposal of interest.
• Partner with TA teams to establish prioritisation of ongoing and planned studies and provide study performance updates to key stakeholders.
• Act as primary contact with the finance team to effectively forecast budget, track invoicing/payment and actual spend by adequately utilizing GSK systems, including the SS system.
• Work with the GSK supplies teams to manage forecast for commercial and clinical supply at the TA level.
• Provide coaching, development and objective setting and prioritisation support for direct/indirect reports or mentees.
• Collaborate across TAs to identify process inefficiencies and lead solution development and implementation.

Basic Qualifications & Skills:

• Master’s degree in a life science or related field.
• Significant experience in clinical trial or study management, with demonstrated accountability for end-to-end study delivery.
• Proven experience working with drug supply chains, including forecasting, coordination with supply teams, and oversight of clinical and/or commercial supply.
• Experience managing external vendors and cross-functional partners within a matrix environment.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and applicable regulatory requirements.

Preferred Qualifications & Skills:

• Experience supporting or managing externally sponsored research, including investigator-initiated or collaborative studies.
• Prior experience in portfolio or asset-level study management, including prioritisation, budget forecasting, and performance reporting across multiple studies.

Closing Date for Applications – 25th September 2026 COB. Please take a copy of the Job Description, as this will not be available post closure of the advert. When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information that you have provided in your cover letter and CV will be used to assess your application.

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.

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.