Clinical Trials Coordinator

2 weeks ago

Airdrie, North Lanarkshire, United Kingdom NHS Scotland Full time
Job Summary

We are seeking a highly skilled and motivated Clinical Trials Practitioner to join our team at NHS Scotland. The successful candidate will provide support for local Principal Investigators who are carrying out Clinical Trials within NHS Scotland, facilitating recruitment into those Clinical Trials, and maintaining adherence to the Clinical Trials Protocols.

Key Responsibilities
  • Support for Local Principal Investigators: Provide administrative support to local Principal Investigators, including coordinating study activities, managing study documentation, and maintaining accurate records.
  • Recruitment and Retention: Facilitate recruitment into Clinical Trials by identifying and engaging potential participants, and providing information and support to ensure successful trial completion.
  • Protocol Adherence: Ensure that all Clinical Trials are conducted in accordance with the approved protocol, and that all necessary documentation is completed and maintained.
  • Study Site Files: Maintain fully up-to-date and accurate Study Site Files for Clinical Trials, including all relevant documentation and records.
  • Research Governance: Ensure that all Clinical Trials are conducted in accordance with Research Governance policies and procedures, and that all necessary approvals are obtained.
  • Collaboration and Communication: Work closely with a wide range of colleagues involved in research within NHS Scotland to develop and increase the Clinical Trials portfolio within the organisation.
  • Training and Development: Develop and deliver training materials to support the development of Clinical Trials skills and knowledge within the organisation.
Requirements
  • Qualifications: First level RGN, or appropriate health-related qualification, and relevant work experience applicable to the Clinical Trials they support.
  • Experience: Experience post RGN registration or post achievement of relevant appropriate health qualification, and relevant work experience applicable to the Clinical Trials they support.
  • Skills: High standard of communication skills, ability to understand the application of Research Governance, and ability to work as part of a team, utilising leadership skills where appropriate.
  • Education: Degree or Post-registration Diploma (or working towards same) or ability to demonstrate equivalent experience to function at degree level.
  • Professional Development: Evidence of continued professional development, and ability to motivate others and work using own initiative.
Desirable Qualifications and Experience
  • Advanced Practice Skills: Evidence of application of advanced practice skills in clinical research and applying clinical judgement providing support at all stages of the clinical research lifecycle.
  • Study Coordination: Experience of coordinating or managing a portfolio of studies, and experience of managing other clinical research staff.
  • Primary Care Experience: Experience working in primary care sites, and comprehensive knowledge of clinical guidelines and standards within clinical research gained through experience working in clinical research in accordance with good clinical practice standards.
  • Legislation and Regulations: Demonstrable knowledge of the EU Clinical Trials Directive and associated UK legislation governing the conduct of Clinical Trials of Investigational Medicinal Products (CTIMPs).
Working Arrangements

This is a part-time post, working 29.7 hours per week. The working pattern for this role is office hours with some flexibility.

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