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This role is not eligible for visa sponsorship. If it is identified that you require sponsorship to undertake this role your application may be withdrawn
We are seeking an enthusiastic individual to provide clinical trial support to the Research and Innovation teams at St George's Hospital, Stafford, and the Redwoods Centre, Shropshire. You will support physical and mental health research in primary care and community settings and coordinate the work of our mobile research unit. The role involves regular travel across the region.
At MPFT we pride ourselves on staff wellbeing and development and can we offer you:
You will work with our partnership team to develop relationships with the voluntary sector and community groups to promote and deliver research, and sustain their research engagement.
You will be responsible for the recruitment, education and monitoring of trial participants as well as the collection and documentation of accurate data, including collection and management of samples.
You must be able to travel across the Trust geography and be willing to drive our mobile research unit, which requires a standard driving licence for manual vehicles.
This is an excellent opportunity for candidates wishing to develop their research expertise to work on a variety of interesting projects within a friendly and supportive team.
You will work autonomously with responsibility for your own portfolio of clinical research studies, with the support of senior staff.
You will be responsible for the recruitment of participants onto clinical trials via different routes in hospital and community settings.
You will play a pivotal role in the delivery of complex research projects, in line with agreed timescales and plans; working with the R&I Research Governance team to ensure that all appropriate approvals have been gained prior to research studies commencing.
You will maintain effective communication between Trust clinical services, primary care and community organisations to ensure safe service delivery.
You will evaluate research protocols, patient information and GP letters and ensure that information about clinical trials is clearly and appropriately communicated to research participants.
You will manage the research related aspect of care for participants of several research studies, which may cover different health specialties.