Responsibilities:
1. To provide support for trials and research studies.
2. To provide administrative and data management support.
3. Assist and support research staff with accurate completion of trial paperwork including processing amendments and checking regulatory approvals.
4. Support the team in preparing documentation for monitoring visits including electronic ordering of medical records, arranging suitable meeting rooms and act as a liaison when monitors are on-site.
5. To manage the Investigator Site File (ISF) for allocated studies.
6. Update the trials databases including EDGE with details of patients screened and recruited to trials/research and any other study information and documents that are required. Training will be provided where necessary.
7. To support local investigators with study set up. To meet with the Principal Investigator (PI) and study team to undertake study feasibility.
8. To assist study team to plan study visit logistics and ensure that studies have all necessary resources.
9. Work alongside research teams to develop working relationships with other multi-disciplinary teams and areas of the Trust involved in clinical research activity.
Experience / Skills:
1. Relevant experience in a NHS/health-related role.
2. Administrative experience.
3. Understanding of Microsoft (including Word and Excel).
4. Ability to work under own initiative and independently without direct supervision.
5. Attention to detail.
6. Able to prioritise tasks and work to a deadline.
7. Good organisational skills.
8. Able to work autonomously or as part of a team.
9. Clear verbal communication.
10. Ability to attend training courses and meetings on and off site.
11. Ability to work in a large busy open plan office.
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