Assistant Research Administrator inPlymouth inPlymouth PUBLISHED
TUE 14 JAN 2025
Key responsibilities include updating quality systems, maintaining regulatory documentation, supporting internal audits, and contributing to the overall administration of the clinical research team. The role requires strong organisational skills, the ability to manage multiple tasks, and a commitment to adhering to standard operational procedures. Candidates with recent relevant experience, particularly existing Trust staff or those with "At Risk" status from the NHS, will be given preference. The position also emphasises the importance of maintaining a respectful and courteous professional demeanor while engaging with patients and colleagues alike.
Research and Development has an opportunity for an enthusiastic Clinical Trials Administrator to work within the Haematology Research team at University Hospitals Plymouth NHS Trust.
The Haematology research team has an extensive portfolio of research covering both malignant and non-malignant haematology in both commercial and non-commercial trials, Phases I - III. The role will be to effectively support in the delivery of these studies.
We are looking for a dynamic, engaging and committed individual who is looking for a new challenge. You will be working in a very busy enthusiastic and supportive team who will also support any training needs.
For further information please contact:
Nicola Crosbie
Specialist research Nurse
The post-holder will work with the research team to provide administrative and clerical support for all aspects of research study delivery across an extensive portfolio of clinical trials.
Preference will be given to internal Trust staff, as well as 'Priority' and 'At Risk' status including NHS At Risk staff throughout Devon who are able to display recent relevant experience as dictated by the Person Specification.
About us
Research and Governance
1. Assist the clinical research team in co-ordinating a portfolio of studies.
2. Participate in Good Clinical Practice (GCP) training and ensures GCP compliance of self and team.
3. Support the team in on-going study coordination including:
Conducting site file maintenance to ensure study essential documents are version controlled and maintained according to regulatory requirements.
Update quality systems to record study information and enrolled patients details.
Coordinate and prepare documents for patient visits.
Respond to patients/carers telephone calls (who may at times be distressed) tactfully and professionally.
Book trial specific investigations and procedures.
Welcome patients to clinic appointments and prepare refreshments if required. Collecting prescriptions or investigation results.
4. Assist in study close out procedures including:
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