Organise and co-ordinate the set-up of NIHR portfolio research. Evaluate patient eligibility for clinical trials, co-ordinating pre-study tests, obtaining results and arranging appropriate appointments according to trial protocol. Ensure that you are working according to principles of ICH GCP and the EU Clinical Trial Directive and adhere to Research Governance standards for clinical research. Act as a resource and support to patients and their carers explaining practical aspects of research studies.
Work with clinical teams to map the patient pathway for each trial. Arrange collection of any samples required as part of the study and ensure safe and appropriate processing and storage of specimens. Liaise with members of the MDTs. Pharmacists, Radiologists and Pathologists to establish procedures for the safe and smooth running of clinical trials.
To maintain accurate records ensuring that confidentiality of information is adhered to. Assist in the review of trial protocols and identify resource implications for the site. This will involve assisting with the negotiation of financial agreements and contracts and ensuring departments are reimbursed as per agreement. To co-ordinate the completion of submissions for local ethical and R&D approval and ensure other legislative requirements are met as required To be responsible for the collection, co-ordination and computerisation of data generated from portfolio studies and the accurate, timely completion of case report forms (CRFs

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