clinical research associate Oxford, England
Job description
Manage your workload and co-ordinate your allocated clinical trials and other research studies together with clinicians, and the clinical research nurses. work with the study coordinator to complete study set up including completion of feasibility requests from both sponsors and R&D and NIHR. Recruit patients from Hepatology clinics and other care settings to the appropriate clinical trials across a broad spectrum of liver conditions with their required follow up. Manage patients care throughout their time in their study whilst evaluating and reporting accurately to senior clinicians and trial sponsors.
Respond to trial queries that are raised in the electronic data capture software by the sponsor within a timely and professional manner. Provide professional and informed advice and support to patients enrolled in all studies and trials. Adhere to the NMC Codes of Conduct, Scope of Professional Practice and Good Clinical Practice at all times. Provide accurate and timely record keeping of case report forms both on paper and sponsor hosted databases.
Act as an autonomous practitioner taking responsibility for clinical decisions where you are competent to do so. Be a mentor for students allocated to the team for placements.
