22/03/2024 | Fulltime | London | CV-Library | £50,000 - £53,000 / Year And laboratory-based role. The Company An industry-leading clinical development services business based in East London. The Role To design, plan and execute lab-based studies as well as conducting data analysis. To run multiple projects. To plan and manage own workload with minimal supervision. A client facing
Save for laterRegister your CV21/03/2024 | Fulltime | Chertsey | CV-Library | £59,000 / Year Of stability, process validation and analytical method validation protocols. - Manage and monitor the progress of validation activities (analytical and manufacturing process) and stability studies, highlighting any out of specification/trend results. - Review batch documentation updates for existing commercial
Save for laterRegister your CV21/03/2024 | Fulltime | Chertsey | CV-Library | £59,000 / Year Of stability, process validation and analytical method validation protocols. - Manage and monitor the progress of validation activities (analytical and manufacturing process) and stability studies, highlighting any out of specification/trend results. - Review batch documentation updates for existing commercial
Save for laterRegister your CV19/02/2024 | Fulltime | Mildenhall | CV-LibraryWith ISO13485 and other medical device regulatory requirements. - Leading, running and moderating use studies such as formative and summative evaluations. - Work closely with the customers and clinical experts to gather relevant information. - Work closely with the project and wider teams to create a device
Save for laterRegister your CV09/04/2024 | Fulltime | Slough | TipTopJob UK | Collecting safety information from multiple potential sources, including spontaneous reports, clinical studies, market research, social media, literature, and license partners. Stay updated on the latest trends and emerging developments in safety data collection. Utilize this knowledge to drive continual
Save for later09/04/2024 | Fulltime | Slough | TipTopJob UK | Development, from Preclinical to Clinical Phase I, II and III studies, to Process Validation support activities. Who you'll work with Due to an exciting and varied portfolio of antibody therapeutic programmes, there is an opportunity for you to work within the Process Data Sciences team as part
Save for laterDon't you miss a job ever again!
Subscribe to all Clinical Studies Officer jobs in the United Kingdom.