Description:
Key Responsibilities include (but not limited to):
- End to end management of clinical trials including obtaining all relevant approvals, budget management, site set up and recruitment, ensure adherence to regulatory and ethical requirements and trial protocols through to follow-up and close down procedures.
- Liaise with the Trial Steering Committee and Independent Data Safety and Monitoring Committee with a particular view on compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements
- Support and guide investigators, researchers, and junior members of staff and engage with external stakeholders to promote the GHTU and its objectives
- Responsible for the recruitment, training, appraisal and supervision of trial team members
- Assist with the planning and delivery of trial specific training programmes to staff at participating sites
- Contribute to the trial’s public profile and assist in updating the protocol and trial related literature