Our client is a world-class cancer research organisation with international ratings of excellence across all of its programmes. They are looking for a Clinical Trials Programme Manager to join their team in Surrey. The role would suit a confident senior trials manager who is interested in cutting-edge research trials, and who would relish the opportunity of working in an academic environment.

Clinical Trials Programme Managers (CTPMs) are each responsible for overseeing a component of the trials portfolio, ensuring trials are initiated and delivered effectively. In addition to dedicated statistical and IT support, each trial has a trial team comprising of trial management, data management and administrative support. The CTPM is responsible for the development and initiation of new trials and for overseeing the trial team, ensuring staff are and suitably trained and supported. In addition, CTPMs are expected to provide scientific or operational expertise and leadership within a defined area of research or trial conduct. This would initially be on a fixed two year contract.

RESPONSIBILITIES/DUTIES

• Development and set up of new studies/sub studies in the context of relevant local, national and international priorities and ongoing research interests
• Overseeing the conduct of a number of studies within the Clinical Trials & Statistics Unit (CTSU) portfolio to ensure their smooth running and progress
• Contributing to CTSU's scientific output, including Drafting clinical trial and methodology publications in conjunction with CIs, trial managers and statisticians
• Line management of a team of trial staff within the agreed portfolio
• Assist with the preparation and facilitation of audits and regulatory inspections
• Proactive member of CTSU's Management Group, attending and contributing to regular management and operational meetings with other senior staff
• Any other duties as may be required, consistent with the nature and grade of the post

REQUIREMENTS

• Minimum of a first degree or equivalent qualification in biomedical sciences or an allied subject (including health care disciplines)
• A postgraduate qualification in biomedical sciences or an allied subject is desirable
• Proven track record working at a senior level (i.e. management team or equivalent) within a research oriented group
• Proven project management / central coordination experience gained in the phase II or III multi-centre trial setting
• Excellent knowledge of the EU Clinical Trials Directive, UK Clinical Trials Regulations, Principles of Good Clinical Practice and research governance framework legislation together with the ability to disseminate the knowledge and information
• Experience of managing, directing and supporting staff
• Excellent organisational and time management skills to manage and deliver a range of tasks and projects to tight deadlines

You must have a valid U.K work permit in order to apply for this role.

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