Description
The Clinical Trial Coordinator will coordinate the delivery of academic Advanced Therapy Investigational Medicinal Product (ATIMP) trials within the haematology team.
The post holder will ensure studies are conducted to the required regulatory, ethical, and quality standards, and to agreed timelines.
Key Responsibilities:
- Coordinate day-to-day management of academic ATIMP trials
- Support patient recruitment, screening, and consent processes
- Undertake source data verification (SDV) and ongoing trial data management
- Perform data extraction and support data cleaning
- Attend and contribute to Data Monitoring Committee (DMC) meetings and Trial Management Group (TMG) meetings
- Assist with regulatory submissions
- Maintain trial documentation in accordance with GCP
- Liaise with multidisciplinary team members, research nurses, and multicentre site staff
- Escalate any protocol deviations, adverse events, or data queries
The second post holder will lead on patient recruitment and trial management for studies within the Lymphoid and Non-Malignant Disease group, while also providing supervision and mentorship to junior trial staff and undertaking sample processing duties.
Benefits:
- Competitive salary £47,951 to £56,863 per annum
- Agenda for Change pay scheme
- Band 6 position
- Fixed term contract for 12 months
- Full-time working pattern
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