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Clinical Programme Director

700.00 - 800.00
Hays Specialist Recruitment Limited

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Clinical Programme Director Oncology exp is essential for Global Pharma, with a proven Science background

Clinical Programme Director required for Global Pharma, Oncology experience is essential along with experience of managing / leading programmes on a global level (early development phase to end).
Ideally candidates will have in-depth knowledge and experience of clinical development of molecules.
Recognised externally as a thought leader and expert within own areas of specialisation. Contributes significantly towards the research strategy addressing business and regulatory issues. Proactively identifies and solves the most complex situations. Operates with no supervision in a complex environment; leads project teams which impact on the organisation at the highest level.

  • In collaboration with Medical Science Director, is accountable for the clinical program strategy, including

innovative approaches to delivery, e.g., new delivery platforms and technology to ensure patient engagement, recruitment and retention.

  • Plans, directs and delivers the operational components of assigned clinical programs from design concept to final CSR, through to study closed and archived within agreed budget, time, quality and aligned KPIs
  • Leads and delivers differentiated and robust operational options for review at Investment Decision Governance interactions
  • Leads operational discussions with external entities including regulatory agencies, preferred partners/suppliers and external collaborators

Responsible for providing strategic and operational input to cross-functional program development plans, data interpretation and accountable for cross-functional leadership roles as delegated from the Global Project Team, e.g., leadership of cross functional product development team activities. Provide expert clinical operational input into: Target Product Profile (TPP), Clinical Development Plan (CDP), Study Synopsis, Clinical Study Protocol, Clinical Study Report, IB, briefing documents, etc., to ensure seamless delivery of programs through effective collaboration
This is 12 month initial contract, based in Cambridge but remote working will be considered for the right person

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