Job Description

Experience required Minimum 2 years post qualification experience Working in the NHS Research experience desirableSuitable for someone who is: Self-motivated, flexible and able to adapt to changing demands, able to process information and interpret accordingly, able to organise own workload and prioritise work as it comes into the department, able to remain calm and professional under pressure and able to respect confidentiality guidelinesKey ResponsibilitiesClinical Work autonomously and assist in the management of a caseload of clinical trial participants whilst working as part of a multi-disciplinary team. Maintain effective communication with people who use our services, carers and professionals to ensure high quality service delivery Identify suitable people who use our services for entry into clinical trials Maintain accurate documentation of participants events in progress notes Ensure people who use our services are fully informed prior to entry into clinical trial programmes Provide ongoing information, education and support to participants (and their significant others) regarding clinical trials and specific trial treatments Ensure that trial specific investigations are undertaken as required by the trial protocol and obtain results in order to establish eligibility and safety to enter the trial Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial Phlebotomy /cannulation training and valid IV drugs/ therapy administration training Monitor treatment toxicity/side effects and initiate changes to treatment or treatment cessation as required by trial protocols Report and record adverse events which occur whilst patients are under trial therapy to the trial co-ordinator/Principal Investigator and relevant local and regulatory authorities Provide continuity of care to participants and their carers throughout the trial programme. Provide specific advice and psychological support as appropriate. Refer to other specialists as required to ensure optimum participants care.



Act as a primary contact point for the trial participant Maintain accurate participants trial documentation, complete Case Report Forms, including the use of electronic data capture systems and ensure relevant information is recorded in participants case notes