16/04/2024 | Fulltime | Didcot, St Peter Port, Douglas | CV-Library | £40,000 - £60,000 / Year Clinical Research Associate, you will be responsible for overseeing trial sites, managing trial data, ensuring compliance with regulatory requirements and maintaining the integrity of study protocols. This is a remote position with occasional site visits. We are looking for an experienced clinical
Save for laterRegister your CV18/04/2024 | Fulltime | Pharma SearchInternational - History - Established in the late 1970's with name changed to Pharmaceutical Research Associates Inc., in 1981 with focus on data management in Virginia, USA. - In 1991, PRA expanded its service offering to include clinical trial management and opened their first European location. - 1996 saw
Save for later02/04/2024 | Fulltime | Abs DataJob title BHF DSC - Associate Director Kidney Data Science Catalyst Company Health Data Research UK Job description Salary This post would be suitable as a secondment Contract Approximately 1 day/week for 3 years Purpose of the post We are looking for a leader who is well connected and highly
Save for later26/04/2024 | Fulltime | Oxfordshire | CV-Library | £25,147 - £27,596 / Year Framework of the SPS policies and procedures. The postholder will also assist in clinically related administration, conduct of audits, collation and analysis of statistics, development of audit and/or research projects, and project work. The successful candidates will have a good honours degree
Save for laterRegister your CV26/04/2024 | Fulltime | London | CV-Library | £29 - £37 / Hour Their understanding the service operates. The SDL can observe and learn the entire site process, participant flow and build confidence in delivery, mitigating the risks associated with new leadership deploying new processes. This additional time also ensures a consistent approach to patient experience and embeds
Save for laterRegister your CV26/04/2024 | Fulltime | London | CV-Library | £29 - £37 / Hour Their understanding the service operates. The SDL can observe and learn the entire site process, participant flow and build confidence in delivery, mitigating the risks associated with new leadership deploying new processes. This additional time also ensures a consistent approach to patient experience and embeds
Save for laterRegister your CV26/04/2024 | Fulltime | Exeter | CV-Library | £29 - £37 / Hour Their understanding the service operates. The SDL can observe and learn the entire site process, participant flow and build confidence in delivery, mitigating the risks associated with new leadership deploying new processes. This additional time also ensures a consistent approach to patient experience and embeds
Save for laterRegister your CV25/04/2024 | Fulltime | Bristol, City of London, City | CV-Library | £45,000 / Year Including budgeting. - Develop operational project plans. - Manage trial associates, investigators, and other trial personnel to ensure personnel are up to date with relevant information or issues. Delegate workloads accordingly Requirements of the Clinical Trials Manager - BSc or equivalent in biomedical
Save for laterRegister your CV25/04/2024 | Fulltime | Darlington | CV-Library | £29 - £37 / Hour Their understanding the service operates. The SDL can observe and learn the entire site process, participant flow and build confidence in delivery, mitigating the risks associated with new leadership deploying new processes. This additional time also ensures a consistent approach to patient experience and embeds
Save for laterRegister your CV25/04/2024 | Fulltime | Clevedon | CV-Library | £29 - £37 / Hour Their understanding the service operates. The SDL can observe and learn the entire site process, participant flow and build confidence in delivery, mitigating the risks associated with new leadership deploying new processes. This additional time also ensures a consistent approach to patient experience and embeds
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