Under the supervision and direction of the consultant, the post holder will be responsible for: Day-to-day provision of medical activity and cover for 1) research participants (patients and healthy volunteers) on the CRF, including those attending the CRF for research visits on a given day as well as any queries generated in between visits; 2) protocol driven activity that requires medical input such as explaining studies and receiving informed consent, physical and neurological exams and specialist assessment using rating scales (protocol-driven), assessment of eligibility for study enrolment; 3) managing the physical and psychiatric care of participants when required and if appropriate; making referrals to appropriate agencies if required. The post holder will be expected to contribute towards CRF Study Coordinator meetings, provide medical input in assessing feasibility, set up and ongoing management of clinical research studies, Standard Operating Procedure (SOP) development and management, and may be asked to undertake venepuncture and cannulation and other medical procedures required by specific studies (training provided if needed). Data recording and management. Under GCP, timely recording of accurate research data and response to data queries is essential. Recording information in the E.H.R such as visit details including consent and any other information relevant to clinical care. Completing all activity recording as required by the CRF Data Manager using the CRF Manager software (training provided). Providing timely correspondence to GPs and other professionals when required. Work collaboratively with other agencies, in particular clinical teams from OHFT (mainly Adult and Older Adult Directorates), Research & Development OHFT, Principal Investigators and other researchers from UO and OHFT, commercial partners (e.g. pharmaceutical company study sponsor) and the local Clinical Research Network. Liaison with researchers at Oxford University Hospitals NHS Foundation Trust may also be required. The post holder will provide daytime medical cover to the level of Immediate Life Support with the other members of the CRF team (training provided). The post holder will be expected to participate in and attend relevant training for research activity, such as GCP and study-specific training. Additional training opportunities supporting the professional development of the post-holder in their clinical research role are encouraged (subject to agreement with the Line manager). The post holder will contribute towards research Patient and Public Involvement and Engagement (PPI/E) activities on the CRF. Workload in terms of numbers of studies and participants seen varies between studies, some studies are much more intensive than others. The workload is usually very predictable as the CRF delivers a clinical research service that is by necessity very tightly timetabled and dependent on closely monitored resource capacity.