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Apply to become a UKTMN Subscriber if you do not currently work within a trial management role but would like to receive updates from the UKTMN
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Select your organisation if there is a match.
Please provide the name of your unit/department
What type of Institution are you based in?
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University/Academic Department
NHS Organisation
Charity/Other
Are you based within a UKCRC Registered CTU?
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Yes
No
Job Title
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Senior Trial Manager
Trial Manager
Trial/Study Coordinator
Trial Assistant/Administrator
Other
If Other, please specify
Location
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East Midlands
East of England
London
North East
North West
Northern Ireland
Oxfordshire
Scotland
South Central
South East
South West
Wales
West Midlands
Yorkshire and the Humber
What is your ethnic group?
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White
Mixed or multiple ethnic groups
Asian or Asian British
Black, Black British, Caribbean or African
Other ethnic group
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What is your gender?
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Female
Male
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Please select which of the core tasks you do
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Contribute to the development of the trial/study protocol
Obtain and maintain relevant trial/study approvals (e.g. ethics, regulatory)
Support and train trial/study staff at CTUs and external sites
Manage essential trial/study documents and amendments (version control, TMF)
Develop, maintain and ensure compliance with trial/study procedures
Contribute to trial/study data management and quality assurance activities
Monitor and manage trial/study recruitment and retention
Monitor trial/study budget
Provide regular updates for all stakeholders
Contribute to trial/study dissemination activities
None of the above
Disease area(s) of expertise
(optional)
Renal and urogenital
Stroke
Skin
Respiratory
Reproductive health and childbirth
Cancer
Cardiovascular
Dementia and neurodegenerative diseases
Diabetes
Ear
Eye
Genetics and congenital disorders
Generic health relevance
Haematology
Infection
Inflammatory and immune system
Injuries and emergencies
Medicines for children
Mental health
Metabolic and endocrine
Musculoskeletal
Neurological
Oral and gastrointestinal
Paediatrics
Primary care
Study area(s) of expertise
(optional)
E-health trials
Non-clinical trials/studies
International trials
Systematic reviews and meta-analyses
Health economics
Qualitative research
Pilot/Feasibility
Observational, cross-sectional
Observational, cohort
Observational, case-control
Observational, diagnostic accuracy
Phase I trials
Phase II trials
Phase III trials
Phase IV trials
CTIMP trials
Non-CTIMP trials
Medical device trials
Surgery trials
Radiotherapy trials
Psychological and Behavioural including Educational intervention trials
Screening programme trials
Diagnostic test trials
Complex intervention trials
Cluster randomised trials
Blinded randomised trials
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