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Job Location | Crymlyn Burrows |
Education | Not Mentioned |
Salary | 26,000 per annum |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent , full-time |
Clinical Trials Assistant, Swansea, full-time, permanent £26kThe RoleThe role is very practical, and you will spend most of your time operating to a very high degree of rigour, under the constraints of time, within our clinical suites. You must be comfortable working in this type of environment.The training programme is prescriptive and demanding. You will be provided with materials and resources, in addition to training videos. You will be expected to undertake several informal and formal competency tests throughout your probationary period. Yourmentor will provide continued support.Following extensive training you will become a key member of the clinical research team responsible for the execution of daily clinical research activities according to Standard Operating Procedures (SOPs), Good Clinical Practice and the applicable ClinicalTrial directives and legislation. You will be solely responsible for performing all aspects of the patient appointment, which will consist of delivering treatments with the investigational product(s), capturing high quality real-time photographs, and performingnon-invasive skin measurements. You will be heavily involved in all aspects of the clinical trial process from study design, recruitment, execution, through to routine close-out activities.The role will involve working independently across multiple clinical suites, and alongside other CTAs in an open plan office; the culture is very friendly, and team based.You will be expected to liaise with study participants both verbally and by written forms of communication, delivering detailed and accurate information about upcoming clinical investigations.You will participate in devising new training resources, including training videos. You may also be asked to participate in footage for marketing and commercial needs.The nature of all work is such that it must be undertaken within the clinical trials facilities and is on a flexible shift pattern that includes evening work.Working under the direction of the Principal Investigator, and reporting to the Director of Clinical Affairs, your responsibilities will include but are not limited to: