Clinical Trial Coordinator
3 weeks ago
Are you an individual who is organised, has an eye for detail and likes to work in a team? If so, you may be the person we are looking for.
The Research & Development Trial Management Unit are seeking an individual who can provide efficient and effective clinical trial coordination, organisation and data management support, for local and multi-centre clinical research trials.
This post offers the potential to progress to a Band 5 position on successful completion of core research competencies, relevant training and successful demonstration of required skills and knowledge (usually within 18-24 months).
To be successful in this post you will need to be able to demonstrate that you have relevant experience in clinical research and data management. You should be an excellent communicator who is able to display initiative, efficient time management, the ability to prioritise workload activities, have a keen eye for detail and possess good literacy and IT skills.
University Hospitals Coventry and Warwickshire NHS Trust, rated as good by the Care Quality Commission, is one of the largest teaching Trusts in the UK.
We are extremely proud of our employees across our hospital sites, with high quality patient care at the heart of everything we do.
Boasting some of the most modern facilities in Western Europe, the Trust is renowned for being at the forefront of research and innovation as part of its blossoming reputation as a worldwide leader in healthcare.
We are proud to be recognised as a Pathway to Excellence ® designated organisation - please click the link for further details about this prestigious award. Pathway To Excellence ® - University Hospitals Coventry & Warwickshire (uhcw.nhs.uk)
By joining our exciting journey, you will form part of a passionate, talented team and will be able to access a wide range of learning and development opportunities. There has never been a better time to join our team.
The Trust is committed to building an organisation that makes full use of the talents, skills, experience, and different perspectives available in our diverse society. We want everyone to feel they are respected, valued, can achieve their potential and receive the most appropriate and relevant care. We will create an environment where the equality and human rights principles of fairness, respect, equality, dignity and autonomy are promoted and are part of the organisation's core values.
Initiation of studies at participating sites, including obtaining NHS permissions, coordinating signing of contracts and arranging and conducting site initiation meetings, ensuring all necessary documentation is in place prior to commencement of the study.
Monitoring compliance of studies with GCP principles, research governance and relevant legislation.
Monitoring study progress at participating sites to ensure compliance with the study protocol and recruitment targets are met.
Providing regular reports on study progress to the Trial Manager and Lead Investigators/study management teams.
Managing the procurement and supply of study consumables and ensuring auditable records are maintained.
Coordinating the processing of study invoices and ensuring accurate and up-to-date records are kept.
Co-ordinating and providing administrative support for study meetings.
Delegated responsibility for maintaining study Trial Master Files in line with ICH GCP guidelines.
Assisting in preparing and maintaining study documentation and ensuring new versions of documents are implemented at sites.
Facilitating the secure storage and archiving of study documentation in accordance with ICH GCP and Research Governance.
For further details of the role please see the attached job description.
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