22/05/2024 | Fulltime | Worms, Gaithersburg, Kaisersla | BioNTech SEResponsibilities of staff and is responsible for recruiting, developing, and retaining talent Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and programming Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality
Save for later22/05/2024 | Fulltime | Worms, Gaithersburg, Darmstadt | BioNTech SEResponsibilities of staff and is responsible for recruiting, developing, and retaining talent Provide guidance to Statistical Programmers on SDTM/ADaM and TLFs specifications development and programming Provide input to database requirements and work closely with Clinical Data Manager to ensure data quality
Save for later25/05/2024 | Fulltime | Newcastle upon Tyne | CV-Library | £22,000 - £25,000 / Year Litigation processes and legal procedures related to clinical negligence. Strong research and analytical skills, with the ability to gather and assess complex medical and legal information. Excellent attention to detail and organisational abilities to manage multiple cases simultaneously. Effective verbal
Save for laterRegister your CV24/05/2024 | Fulltime | Shipley | CV-Library | £26 / Hour Booking. Working hours Monday – Friday, 37.5 hours per week (hours flexible between 8am and 8pm). Part time will be considered. Main Duties Manage a caseload of clients in the community Input data in the clinical information system e.g. including risk assessments, care plans, CPA, crisis
Save for laterRegister your CV24/05/2024 | Fulltime | Oxford | CV-LibraryThemselves on innovation, quality and excellence. Responsibilities - - Production of prototypes, pre-clinical and clinical trial products for projects in ISO 8 cleanroom facility. Manufacturing batches to time and GMP standards. - Cleaning and calibration of facilities equipment - Cleaning and helping
Save for laterRegister your CV24/05/2024 | Fulltime | Cambridge | CV-LibraryMedical Device business) of GxP and Quality related regulations and standards - Essential ISO 9001, ISO 13485, GCP, - Desirable ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor (external audits) - Experience of an Electronic Document Management System Skills - Good inter
Save for laterRegister your CV24/05/2024 | Parttime | London | CV-Library | £36 / Hour PCM TRIALS provides quality, in-home clinical trial visits for our Sponsors and CROs partners. We're the only company that hires, certifies, tests, manages and trains our own Certified Mobile Research Nurses (CMRNs) in study protocol standards. Our mission is to bring clinical trial visits
Save for laterRegister your CV23/05/2024 | Fulltime | Southampton | CV-Library | £22,816 - £24,366 / Year Process, and distribute medicines, including Controlled Drugs (CDs) within the Trust - Driving and delivering medication to designated locations within the Trust region - Support the Trust compliance to legislative and governance requirements pertaining to medicines including CDs, clinical trials
Save for laterRegister your CV23/05/2024 | Fulltime | London | CV-LibraryQuality support for other functions within the business e.g. R&D - clinical trial sample testing - process development teams as required - Promote quality culture and one of continuous improvement within team What are we looking for? - Min 2 years’ experience or equivalent experience working in a Quality
Save for laterRegister your CV21/05/2024 | Fulltime | Hillingdon | CV-Library | - £48 / Hour Considerations in developing strategy ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders. Manage regulatory submissions (e.g. clinical trial and marketing applications) for products in compliance with global filing plans and local regulatory
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