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Would you like to join our CTU?

clinical trials data entry clerk/general assistant

NDORMS, Oxford Trauma, Kadoorie Critical Care Research Centre, John Radcliffe Hospital, Oxford, OX3 9DU

Grade 3: £20,092- £22,847 per annum 

We are seeking a reliable and enthusiastic Clinical Trials Data Entry Clerk / General Assistant to provide data collection and entry support for the Oxford Trauma group, based at the Kadoorie Centre, John Radcliffe Hospital, Oxford. This is an exciting opportunity to join a growing department and provide data assistance to clinical trials and research projects.
 
As a Clinical Trials Data Entry Clerk / General Assistant your primary responsibilities will be to provide assistance with data entry for trials and research projects, perform follow-up data collection where needed and organise research data from various sources. Other duties will include assisting the trial management team with missing data/quality checks, supporting the activities of the trial management team in trial-related administrative activities, assisting with the development of study databases, maintaining accurate records, ensuring confidentiality and security of data at all times and dealing with trial-related telephone queries and post.

For further details follow this link

Closing Date & Time: 21-Jan-2022 12:00

 

programmer

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, Windmill Road, Oxford, OX3 7LD

Grade 5: £26,341 - £31,406 per annum

We have an exciting opportunity for an enthusiastic and reliable Programmer to join the Oxford Trauma group, based at the Kadoorie Centre, John Radcliffe Hospital, Oxford. This is an interesting opportunity to join a growing department, supporting the clinical research undertaken by Oxford Trauma and Emergency Care (OTEC) group by providing technical solutions and support for the research team and provide data assistance to clinical trials and research projects.

As Programmer your primary responsibilities will be to assist the Senior Research Information Specialist and other specialist staff to design, develop and support software and processes to support Oxford Trauma research. You will carry out data cleaning and bug fixes, assist in the generation and development of data collection system specifications and test and implement software in consultation with users. You will also assist in the ongoing maintenance of the data collection systems used by OTEC and be involved in writing, reviewing, and running test scripts and other support documentation for trial databases.

For further details follow this link

Closing Date & Time: 24-Jan-2022 12:00

 

 

clinical trials administrative coordinator

NDORMS, Oxford Trauma, Kadoorie Critical Care Research Centre, John Radcliffe Hospital, Oxford, OX3 9DU
Grade 5: £26,341 - £31,406 p.a.
We have an exciting opportunity for a Clinical Trials Administrative Coordinator to join the Oxford Trauma group at the Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, to be based at the Kadoorie Critical Care Centre, John Radcliffe Hospital, Oxford.
 
As a Clinical Trials Administrative Coordinator, you will carry out day-to-day administrative coordination of project(s) with minimum supervision, reporting problems immediately, and providing updates to the Trial Manager. You will work within the Oxford Clinical Trials Research Unit (OCTRU) Standard Operating Procedures (SOPs). You will be responsible for monitoring of your own project and related junior staff to ensure quality assurance compliance and you will provide administrative support for meetings and support to the Trial Manager in the development of case report forms and documents.
You must be educated to A-Level standard (or equivalent administrative qualifications/experience). You will have excellent IT literacy, including a strong working knowledge of Word and Excel, with the ability to create and use spreadsheet applications. Evidence of following and working to detailed written instructions associated with quality control or compliance, and ability to maintain clear and accurate records and demonstrable knowledge of data management, research quality management and monitoring activities are essential. Understanding of clinical governance, familiarity with IRAS and experience of working within a registered clinical trials unit would be desirable.
For further details follow this link

Closing Date & Time: 24-Jan-2022 12:00