Global Clinical Program Delivery Director
3 weeks ago
The Global Clinical Program Delivery Director will be a key member of the Clinical Operations Leadership Team at GSK, contributing to the overall strategy and direction of ClinOps. This role will define the future vision for the team and ensure successful project delivery and outcomes across the organisation.
The successful candidate will lead a global team responsible for the operational delivery of the entire end-to-end Pharma clinical portfolio. They will ensure delivery of key clinical development plan progression targets, from design through to submission.
This role will own the enterprise study sourcing strategy, in partnership with the Head of Vaccine Program Delivery, to ensure teams have the requisite talent and expertise to deliver the pipeline utilising the internal GSK delivery model or outsourcing to strategic partners.
The Global Clinical Program Delivery Director will also be responsible for embedding innovative approaches to drive protocol optimisation and to accelerate recruitment and development timelines across the life cycle of a study/asset.
Additionally, this role will enable close synergies between clinical scientists, MDL, medical writers to complete key strategy documents and ensure timely delivery of high-quality submissions.
The ideal candidate will have a strong track record of establishing and executing strategic vision for a global function, ensuring successful project delivery and outcomes across the organisation.
They will have experience in clinical operations, including study/asset leadership, data and site management, and driving transformation across organisational changes, digital uplift and accelerating ways of working.
The Global Clinical Program Delivery Director will be a key ambassador for GSK's Clinical Operations function, promoting a culture of innovation, collaboration and excellence.
- Provide strategic leadership, management and single point of accountability for all aspects of Pharma Clinical Program Delivery worldwide.
- Lead and direct a large, global, cross-functional organisation of professional and highly experienced clinical staff.
- Embed innovative approaches to drive protocol optimisation and to accelerate recruitment and development timelines.
- Enable close synergies between clinical scientists, MDL, medical writers to complete key strategy documents.
- Embed clinical planning as a core capability within the asset lead and SDL community.
- Create a culture within the organisation that values sharing best practices, fostering a sense of community, identification and development of key talent, innovation and problem-solving.
- Understand quality trends/issues as it relates to delivery of clinical trials and take a more holistic approach to CAPA development and implementation.
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