13389 - Assistant Trial Manager
| Dyddiad hysbysebu: | 17 Tachwedd 2025 |
|---|---|
| Cyflog: | £34,610 i £39,906 bob blwyddyn, pro rata |
| Oriau: | Rhan Amser |
| Dyddiad cau: | 15 Rhagfyr 2025 |
| Lleoliad: | Edinburgh, Scotland |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | University of Edinburgh |
| Math o swydd: | Dros dro |
| Cyfeirnod swydd: | 13389 |
Crynodeb
Grade UE06: £34,610 to £39,906 per annum, pro-rata if part time
CMVM / Centre for Clinical Brain Sciences
Part-time: 21 hours per week
Fixed term: 24 months
We seek an energetic, organised, motivated Assistant Trial Manager for the LACunar Intervention Trial 3 (LACI-3) that aims to improve outcomes after small vessel stroke funded by the National Institutes of Health and Care Research (NIHR).
The Opportunity:
LACI-3 is the largest and only Phase 3 trial in small vessel (lacunar) stroke in the world, a major cause of stroke and vascular dementia, currently with no effective treatment.
As the Trial Research Data Administrator for LACI-3, you will be responsible for monitoring data accuracy and completeness in real time, liaising with sites and other LACI-3 team members amongst other factors. Your role will be crucial to ensure high-quality, complete and successful data collection for this high-profile trial.
You will work closely with the LACI-3 Trial Manager and central teams at the Universities of Edinburgh and Nottingham, and Site teams. You will assist the Trial Manager and Team with other activities, as appropriate to the stage of LACI-3, including managing the trial email inbox, providing trial materials to sites, and assisting Follow-up Co-ordinators.
This post is full or part-time (minimum 21 hours per week); however, we may consider flexible working patterns. The post is primarily office based, but we may consider requests for a mix of office and home (hybrid) working (on a non-contractual basis).
The salary for this post is UE06
Your skills and attributes for success:
You will have experience in clinical trials data management and research administration;
You will have excellent organisational and data accuracy skills;
You will have experience of multicentre trials including liaison with site staff and primary care;
You will have up to date knowledge of research ethics and R&D principles, and of Good Clinical Practice with an up-to-date GCP certificate.
CMVM / Centre for Clinical Brain Sciences
Part-time: 21 hours per week
Fixed term: 24 months
We seek an energetic, organised, motivated Assistant Trial Manager for the LACunar Intervention Trial 3 (LACI-3) that aims to improve outcomes after small vessel stroke funded by the National Institutes of Health and Care Research (NIHR).
The Opportunity:
LACI-3 is the largest and only Phase 3 trial in small vessel (lacunar) stroke in the world, a major cause of stroke and vascular dementia, currently with no effective treatment.
As the Trial Research Data Administrator for LACI-3, you will be responsible for monitoring data accuracy and completeness in real time, liaising with sites and other LACI-3 team members amongst other factors. Your role will be crucial to ensure high-quality, complete and successful data collection for this high-profile trial.
You will work closely with the LACI-3 Trial Manager and central teams at the Universities of Edinburgh and Nottingham, and Site teams. You will assist the Trial Manager and Team with other activities, as appropriate to the stage of LACI-3, including managing the trial email inbox, providing trial materials to sites, and assisting Follow-up Co-ordinators.
This post is full or part-time (minimum 21 hours per week); however, we may consider flexible working patterns. The post is primarily office based, but we may consider requests for a mix of office and home (hybrid) working (on a non-contractual basis).
The salary for this post is UE06
Your skills and attributes for success:
You will have experience in clinical trials data management and research administration;
You will have excellent organisational and data accuracy skills;
You will have experience of multicentre trials including liaison with site staff and primary care;
You will have up to date knowledge of research ethics and R&D principles, and of Good Clinical Practice with an up-to-date GCP certificate.