Role Overview
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 portfolio delivery leadership at an Asset level, the Lead will coordinate review and outcome dissemination for Investigator Initiated Sponsored (IIS) and Supported Collaborative Studies (SCS) proposals for the TA. They will deliver the asset’s study portfolio, including milestone and budget forecasting and management, prioritisation of studies and leading communication with key stakeholders. The 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.
- Manage studies in accordance with GSK SOPs and relevant legislations, study timelines and supply management as well as operational point of contact for the external Study Sponsor and internal stakeholders.
- Provide coaching, development and objective setting and prioritization support for direct/ indirect reports or mentees.
- Collaborate across TAs to identify process inefficiencies and lead solution development and implementation.
Basic Qualifications & Skills
- Bachelor’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
- Master’s degree in a life science or related field.
- 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.
Benefits
Competitive salary, annual bonus based on company performance, comprehensive healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
Equal Opportunity Employer
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.
Accessibility and Adjustments
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 the opportunities available. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities, contact us at UKRecruitment.Adjustments@gsk.com. Please note that if your enquiry does not relate to adjustments, we will not be able to support you through these channels.
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For US Licensed Healthcare Professionals or Healthcare Professionals defined by the laws of the state issuing your license, GSK may be required to capture and report expenses incurred on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements.
