Trial Coordination

As an Senior Clinical Trial Manager your main duties will include

• Leading the set-up, conduct and closure of multi-centre randomised controlled trials and actively contribute to the design, from a trial co-ordination, regulatory and logistics perspective;
• Managing projects, making of day-to-day decisions and highlighting critical issues to the senior team, adhering to milestones and resources outlined in the grant application and supervising and managing trial co-ordination staff;
• Maintaining a thorough and up-to-date understanding and working knowledge of legislation, guidance and local and national initiatives relating to clinical research and applying this knowledge through working practices on the projects you manage;
• Working in partnership with the Divisional Director, Principal Statistician and Head of Trial Management to develop grant applications and implement high quality randomised controlled trials;
• Establishing and maintaining professional relationships with collaborators including funders, staff from other trials units, clinicians, professors, relevant laboratory and research staff at both national and international centres;
• Actively contributing to the development of systems and processes through involvement in Working Groups and development or amendment of associated documentation;
• Contributing to high quality publications in peer-reviewed clinical and methodological journals and presenting research, and/or issues in trial design and conduct, at local, national and international meetings and conferences;
• Delivering relevant training sessions, both internally and externally.