Supported Studies Asset Study Delivery Lead

Asset Study Delivery Lead

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. Accountability is for the complete Supported Study (SS) portfolio, including milestone and budget forecasting, study prioritisation, and communication with key stakeholders.

Responsibilities

• Lead coordination of proposal submissions and facilitation of the proposal review with matrix key stakeholders (LOC, safety, supply, legal, medical affairs, stats, and external investigators), and communicate the review outcome to external and internal stakeholders.
• Ensure IdeaPoint and Veeva are updated with 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 using GSK systems, including the SS system.
• Work with 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, overseeing study timelines, supply management, and serving as the operational point of contact for the external Study Sponsor and internal stakeholders.
• 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.

Qualifications

• 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

• 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.

Closing Date for Applications - 5th July 2026 COB

Equal Opportunity Statement

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.