15/04/2024 | Fulltime | City of London, Dundee, Bristo | 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 CV15/04/2024 | Fulltime | London | CV-Library | £14 / Hour To support your job search and offer expert interview tips Duties of the role Manage the agency database(s) and check consistency between public registers Inputting applications on the Agency databases and supporting the application specialists with allocation of both clinical trials applications
Save for laterRegister your CV12/04/2024 | Fulltime | Cambridge | CV-Library | £100,000 - £150,000 / Year In growing the value of the company by defining external opportunities for the platform, through monitoring the Lung and Heart clinical trials market. Key contributor to drive the delivery of the company's growth and business plan. Collaborating with the senior leadership team to deliver the end-to-end deal
Save for laterRegister your CV10/04/2024 | Fulltime | London | CV-Library | £46,000 / Year For improvement. There may be some travel involved with this role. Skills & Experience for Success Experience in project management or clinical trials setup within healthcare or research settings. Strong interpersonal skills with the ability to build and maintain relationships with diverse stakeholders
Save for laterRegister your CV10/04/2024 | Fulltime | England | CV-Library | £55,000 - £60,000 / Year clinical trials and product utilisation. - Creating detailed records of all contacts and activities in a CRM - Supporting post market surveillance data gathering - Attending and presenting clinical and commercial updates at internal company meetings. - Monitoring clinical activity - Keeping up to date
Save for laterRegister your CV08/04/2024 | Fulltime | London | CV-Library | £80,000 - £90,000 / Year And performs complex ǪA activities involving evaluating and reviewing processes to ensure manufacturing, testing and clinical trials activities comply with GMP, GCP, HTA and other regulatory requirements relating to manufacture and clinical trials for cellular therapies and AT(I)MPs including. • Identifies
Save for laterRegister your CV04/04/2024 | Fulltime | Manchester | CV-Library | £55,000 / Year Building strong relationships with Hospitals, Clinicians, and other key stakeholder groups. - Working in collaboration with the Product Manager and Nurse Clinical specialist(s) to provide a detailed understanding of the UK market - Delivering training to practice staff and nurses to support clinical trials
Save for laterRegister your CV04/04/2024 | Fulltime | Birmingham | CV-Library | £55,000 / Year Building strong relationships with Hospitals, Clinicians, and other key stakeholder groups. - Working in collaboration with the Product Manager and Nurse Clinical specialist(s) to provide a detailed understanding of the UK market - Delivering training to practice staff and nurses to support clinical trials
Save for laterRegister your CV03/04/2024 | Fulltime | Nottingham | CV-LibraryVarious systems and databases to analyze risk related to trial quality/performance and compliance and identify trends and early warning signals. Analytical problem solving/critical thinking abilities and experience. Working knowledge of clinical drug development process as well as ICH, GCP guidelines
Save for laterRegister your CV03/04/2024 | Fulltime | Ellesmere Port | CV-LibraryParticipants and data are safeguarded in compliance with applicable regulatory requirements and best practice. Work with training and monitoring colleagues, to implement, review and maintain tracking of incidents within the organisation, including those related to clinical trials, advising on Opportunities
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