Global Clinical Program Delivery Director

4 weeks ago


Mississauga, Ontario, Canada GlaxoSmithKline Full time

The Vice President of Pharma Clinical Program Delivery will be a key member of the Clinical Operations Leadership Team, contributing to the overall running of ClinOps and defining the future strategy. This role will also contribute to Development Review Boards to support governance decision making for new medicines.

The VP of Pharma Clinical Program Delivery will lead a global team, accountable for the operational delivery of the entire end-to-end Pharma clinical portfolio. This includes ensuring delivery of key clinical development plan progression targets, from design through to submission.

This position 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. The VP will also effectively partner with Research Unit leadership teams, MDLs/EDLs, Clinical Sciences, Supply Chain, Regulatory, ClinOps functions, and other senior stakeholders to embed solutions to optimize operational delivery of development plans and accelerate cycle times.

Additionally, the VP of Pharma Clinical Program Delivery will enhance relationships with GSK's strategic partners to improve delivery, productivity, and vendor performance.

  1. Provide strategic leadership, management, and single point of accountability for all aspects of Pharma Clinical Program Delivery worldwide to ensure delivery of key progression targets and optimum alignment with stakeholders.
  2. Lead and direct a large, global, cross-functional organization of professional and highly experienced clinical staff, including aspects of training and development, performance management, career development, and deployment to projects and work activities consistent with business requirements.
  3. Embed innovative approaches to drive protocol optimization and accelerate recruitment and development timelines across the life cycle of a study/asset, with a goal to reduce amendments prior to FSFV and accelerate start-up cycle times.
  4. Embed the principles of CRO excellence to improve productivity and quality from strategic partners.
  5. Enable close synergies between clinical scientists, MDL, medical writers to complete key strategy documents and ensure timely delivery of high-quality submissions.
  6. Accountable for the enterprise clinical sourcing strategy and responsible for re-assessing strategic partners to ensure strategy is Fit for Purpose and aligns with future pipeline.
  7. Embed clinical planning as a core capability within the asset lead and SDL community to optimize plans with clear mitigation strategies.
  8. Create a culture that values sharing best practices, fostering a sense of community, identifying and developing key talent, innovation, and problem-solving in an increasingly challenging environment.
  9. Understand quality trends/issues as it relates to delivery of clinical trials and take a holistic approach to CAPA development and implementation.
  10. Support maintenance and regulatory authority inspection readiness for the entire R&D pharma & Franchise clinical portfolios.
Key Qualifications:
  1. Bachelor's degree in Sciences or Business.
  2. Experience in establishing and executing strategic vision for a global function, ensuring successful project delivery and outcomes across the organization.
  3. Experience in clinical operations, including study/asset leadership, data and site management.
  4. Experience driving transformation across organizational changes, digital uplift, and accelerating ways of working.
Preferred Qualifications:
  1. Master's degree or PhD.
  2. Project Management skills/experience.
  3. Effective communication, negotiation, and presentation skills at various senior levels of the organization.


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