Clinical Trial Project Coordinator Jobs in Southampton, England | Glassdoor
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Clinical Trial Project Coordinator Jobs in Southampton, England

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  • 3.1
    Clinical Professionals – United Kingdom
    Today 3hr
    CPM, CTM, clinical research, clinical trial, clinical study, clinical studies, pharma, pharmaceutical, clinical project management… sciences, CPM, clinical management, clinical trial manager, senior clinical trial manager, senior clinical trial management, senior…
  • 4.1
    University of Southampton – Southampton, England
    2 days ago 2d
    Trial Coordinator/ Research Manager - MSRGFOS - Faculty of Health SciencesLocation: Highfield Campus Salary: £29,301 to £36,… note: Upon appointment the post holder will be known as a Trial Coordinator. Applicants are strongly advised to speak informally…
  • 3.1
    ICON – Eastleigh, England
    4 days ago 4d
    regulatory reporting requirements for safety reporting in clinical trials. Ensure all ICON, Sponsor, and regulatory timeframes… Role As a Drug Safety Coordinator, you will be expected to; Lead projects and take on project management activities.…
  • 4.1
    University of Southampton – Southampton, England
    Today 2hr
    for Health Research) Evaluation, Trials and Studies Coordinating Centre (NETSCC). A coordinating centre managing and maximising… team Part time, 0.6 fte Assistant Research Manager, NIHR Clinical Trials Unit Support Funding – fixed term contract until 31 March…
  • 3.3
    NHS Jobs – Bournemouth, England
    9 days ago 9d
    supervision of our clinical trials data team. The successful candidate will be responsible for all aspects of clinical trials data management… Research Directorate. Based in the Clinical Trials Office team and sharing our passion for clinical research, you will be required…
  • 3.1
    ICON – Eastleigh, England
    24 days ago 24d
    regulatory reporting requirements for safety reporting in clinical trials. Ensure all ICON, Sponsor, and regulatory timeframes… expected to prepare regulatory documentation packets and coordinate the timely completion and submission of required reports to…
  • 3.1
    ICON – Eastleigh, England
    10 days ago 10d
    regulatory reporting requirements for safety reporting in clinical trials. Ensure all ICON, Sponsor, and regulatory timeframes… improvement Supervise maintenance of project drug safety files as regionally applicable Coordinate any committee activities as applicable…
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