Clinical Trial Practitioner
- Assist in carrying out research studies according to GCP standards in strict accordance with
the protocol and with local Standard Operating Procedures. - Support accurate and timely feasibility assessments of proposed studies
- Ensure studies are recruited to time and target set out in contract
- Support research studies in accordance to NIHR benchmark; recruitment of first patient within 30days of NHS permission.
- Support the process of gaining relevant NHS permissions for research studies.
- Prepare patient documentation for research-related treatment clinics, accurate records of patient care, maintain source data and Case Report Forms and all other trial documents in a manner conducive to audit.
- Develop and maintain knowledge of Research Governance, GCP and current legislation relating to research, and to keep up-to-date with changes and new developments.
- Develop an understanding of the roles of the Integrated Research Application System (IRAS) Co-ordinated System for Gaining NHS Permissions (CSP), Research Management & Governance arrangements and Research Ethics Committees.
- Health care Qualification
- Or Life science degree
- Understanding of clinical research methodology
- Clinical Research experience
- Experience of managing complex information or projects
- Competent Computer skills
- Working in the NHS
- Participation in consent process for patients entering clinical research
- Experience of working independently and as part of a team
- Ability to cope with work pressures and manage time effectively
- Demonstrate effective verbal and written communication.
- Ability to work using own initiative but also to know when to seek assistance and guidance.
- Ability to innovate and respond to change
- Job Description (PDF, 949.3KB)
- Functional requirements (PDF, 292.9KB)
- Our Strategy 2023-25 (PDF, 230.4KB)
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