Trial Coordinator - Stafford, United Kingdom - Midlands Partnership University NHS Foundation Trust
3 weeks ago
Description
We are seeking to recruit a Band 6 Trial Coordinator to work within our friendly and supportive research delivery teamThe team deliver a range of studies in various specialty areas within mental health, physical health and vaccines.
You will be responsible for the coordination of a range of clinical trials, ensuring they are safely and efficiently set up and delivered in accordance with Trust and regulatory requirements.
- You will work alongside research nurses and practitioners to coordinate of a range of clinical trials and research studies, ensuring they are safely and efficiently set up and delivered
- You will be the first point of contact within the research delivery team, liaising closely with support departments such as pharmacy, imaging and other clinical teams across the Trust, as well as sponsor organisations
- You will be the main liaison between the delivery and research governance teams.
- You will monitor delivery of those studies, ensuring time and target metrics are met by the delivery team.
MPFT provides physical and mental health care, learning disability, and adult social care services across Staffordshire, Stoke-on-Trent, Shropshire, and Telford & Wrekin.
By joining MPFT you will become part of a diverse and inclusive team who are empowered and supported to deliver care in a way which is consistent with our values:
- putting people at the heart of what we do
- delivering better health, better care in partnership
We are embedding values based and inclusive recruitment practices to ensure that all applicants, from any backgrounds, from under-represented groups, such as black, Asian or other ethnic groups, individuals with a disability, or LGBTQ+ individuals.
We will support your career development and progression. Membership of the excellent NHS pension scheme, generous maternity, paternity, adoption leave, pay and the option for flexible working.
You will receive up to 27 days annual leave (increasing to 33 days) and the opportunity to purchase additional annual leave.
We are also proud to have a choice of staff networks that help you meet like-minded people.- Work autonomously to manage your own caseload of studies, with the support of research team leaders and senior management.
- Ensure the set up and delivery of complex research studies, in line with agreed timescales and plans
- Assess trial protocols and identify the delivery requirements of each study, including any safety, regulatory and logístical issues; formulate plans for study specific training, standard operating procedures and risk assessments
- Monitor the performance of studies once open against recruitment targets; act as point of contact for sponsor organisations and study monitors, coordinate reporting of key data such as adverse events, protocol deviations and other key metrics
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