At a Glance
- Tasks: Lead the delivery of clinical studies and manage key stakeholder communications.
- Company: Join a leading global healthcare company committed to innovation.
- Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on career development and equal opportunity.
- Why this job: Make a real impact in healthcare by managing important clinical studies.
- Qualifications: Bachelor’s degree in life sciences and experience in clinical trial management.
The predicted salary is between 60000 - 75000 £ per year.
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
Supported Studies Asset Study Delivery Lead employer: Dormont Manufacturing Co
At GSK, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of the life sciences sector. Our commitment to employee growth is evident through comprehensive training programmes and mentorship opportunities, ensuring that our team members thrive in their careers while contributing to meaningful research that impacts global health. Located in a vibrant area, we provide a supportive environment where diverse perspectives are valued, making GSK not just a workplace, but a community dedicated to advancing healthcare.
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We think this is how you could land Supported Studies Asset Study Delivery Lead
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We think you need these skills to ace Supported Studies Asset Study Delivery Lead
Some tips for your application 🫡
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Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Dormont Manufacturing Co that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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