26 to 30 of 30 Clinical Data Management Jobs in the UK

execution of programs in statistical programming languages within project. Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations. Create complex programs that meet regulatory and company standards to permit efficient programming, reporting, and review, utilizing statistical programming languages (e.g … validation documentation to meet regulatory and company standards are consistently structured to permit efficient programming, reporting, and review. Perform complex analysis in response to data requests in collaboration with designated statistician. Collaborate with CDM (Clinical Data Management) and designated statistician to review draft CRFs (Case Report ...

oversight professional with a technical mindset, strong communication skills, and deep knowledge of SDTM. This remote role supports study design, CRF annotation, and vendor management across Europe and South Africa. You will oversee SDTM deliverables throughout the study lifecycle, map data, review CRF modules, and ensure regulatory compliance. … Experience with SAS and clinical data management is valued; English fluency is required. #J-18808-Ljbffr ...

Edwards Lifesciences is seeking a Statistical Programmer to drive critical analyses for clinical reports and presentations. You will develop complex datasets and outputs while ensuring regulatory compliance across modeling and reporting tasks. This on-site role requires a strong background in statistics and SAS, with a move toward collaborating … with the Clinical Data Management team to review CRFs and specifications. California-based, on-site location. #J-18808-Ljbffr ...

Optos PLC in Dunfermline is seeking a Senior Software Engineer to develop and enhance retinal imaging workflows and clinical data management solutions. You will focus on UI and application layer development, while integrating with Optos' image and metadata platform. The role requires collaboration with Product, DevOps ...

projects for a renowned, innovative and global top pharmaceutical company. You will be involved in liaising with the entire study team as needed, including Clinical, Medical Writing, Safety and Biometrics. It is a great opportunity to see more how this works from a Big Pharma perspective, whilst still being … relevant field such as mathematics, life sciences, statistics, computer sciences, etc. In lieu of the above: professional experience in statistical programming within clinical trials in a biotech, CRO or pharmaceutical company. Solid experience with complex clinical trials (minimum 5 years) and the corresponding data sets content (safety ...