25/04/2024 | Fulltime | Bristol | CV-Library | £45,000 / Year Studies. - Author Clinical Investigation Plans (CIP) and Final Study Reports (FSR) - Statistically analyse clinical data - Draft clinical manuscripts for publication - Prepare abstracts, power-point presentations and posters for submission to scientific conferences. - Understand how clinical data can best
Save for laterRegister your CV15/04/2024 | Fulltime | City of London | CV-Library | £30,000 / Year And template documentation, as deemed appropriate Requirements of the Research Manager - Solid degree in scientific subject. - Experience in a clinical research setting; proven clinical trial experience. - Experience in Phase I-IV trials; Phase II - III is preferred. - Working knowledge of EU Clinical Trials
Save for laterRegister your CV03/04/2024 | Fulltime | Leominster | CV-LibraryWith the preparation of Clinical Evaluation Reports with input from scientists and clinicians. - Review documentation, prepare a gap analysis and write documentation to fill those gaps for regulatory submissions. - Submit and maintain regulatory documents as required and Liaise with external organisations regarding
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