Location: | London, Hybrid |
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Salary: | £52,762 to £62,035 |
Hours: | Full Time |
Contract Type: | Permanent |
Placed On: | 17th March 2025 |
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Closes: | 13th April 2025 |
Job Ref: | B02-08228 |
About us
PRIMENT Clinical Trials Unit mission is to advance the quality, range and design of clinical trials in primary care, mental health and community settings in order to improve the health of the population. PRIMENT CTU is a partnership between 3 UCL departments:
PRIMENT CTU conducts high quality randomised trials and related studies in mental health and primary care. The unit has a particular focus on mental health and behavioural change interventions. PRIMENT CTU collaborates with internal and external researchers to develop and/or evaluate complex interventions in primary care, psychiatric and community settings. PRIMENT CTU is a UK Clinical Research Collaboration (UKCRC) registered clinical trials unit. UKCRC registration recognises the CTU's strengths in conducting major trials and other large, well-designed studies.
PRIMENT CTU receives National Institute for Health Research (NIHR) CTU support funding. This funding has been awarded to support the unit in developing and supporting NIHR trials. The Directors of the CTU at UCL are Professor Irwin Nazareth and Professor Greta Rait.
The Research Department of Primary Care and Population Health is part of the Institute of Epidemiology and Health Care and is co-led by Professor Greta Rait and Professor Kate Walters. Further information can be found at: www.ucl.ac.uk/epidemiology-health-care/research/pcph
About the role
The primary role of the post holder is to establish, implement and deliver high quality data management service to collaborating academics and clinicians both within UCL and externally. The post holder will lead on the delivery and implementation of Priment Clinical Trials Unit (CTU) Data management strategy required to support the CTU clinical trials portfolio, which consists of both CTIMP and non-CTIMP studies. The post holder will also have duties in delivering trial-specific clinical data management systems.
About you
The post holder must have a degree or equivalent, in a subject allied to information technology, computer science, or mathematics and have significant experience of data management in clinical trials.
They must have a good understanding of Good Clinical Practice (GCP) and current regulatory requirements relating to data management in clinical trials and demonstrates strong leadership skills.
The successful candidate must be able to use Microsoft word and Excel at an advanced level, have good knowledge of SQL and other database concepts and has experience with the design, build, testing, and using Clinical Trial Data management systems.
Customer advert reference: B02-08228
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