7 of 7 Permanent Clinical Data Management Jobs in the South East

each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.Job Function: Data Analytics & Computational SciencesJob Sub Function: BiostatisticsJob Category:Scientific/TechnologyAll Job Posting Locations:High Wycombe, Buckinghamshire, United KingdomJob Description:Position SummaryThe Experienced Clinical Programmer is an experienced clinical trial programmer with in-depth knowledge in industry standard and complex data structures, programming languages, and/or reporting solutions with proven technical capabilities in leading clinical trial activities and/or teams in accordance with departmental processes and procedures.The position ...

strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments)Setup/Program QTL, KRI and Data Quality Assessments according to the study CMPRefresh the Centralized Monitoring … enable signal identificationGenerate and maintain the Centralized Monitoring Platform specifications document and file it in eTMFReview and understanding of protocol is keyUnderstand the data sources for the study, the data transfer specifications and the data structureExecute and document peer-review of CM platform setup done by other ...

someone with a technical mindset, strong communication skills, and a good understanding of SDTM.Experience in Study Design, CRF annotation, CDISC standards, and vendor management will be key for success in this position. The role can be performed remotely from a number of countries in Europe or South Africa.As part … deliverables.Main responsibilities include:• Collaborate with Sponsor colleagues and CRO Partners to review CRF design and compliance into standard and SDTM.• In collaboration with Study Data Leads ensure the planning for data receipt and its oversight throughout the duration of assigned clinical trials• Program reports and contribute ...

Clinical Trial Designer will create high quality data collection tools for new clinical trials and facilitate activities related to the design, development, documentation, testing and implementation of clinical eCRF databases. Design of eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio … expected. In addition, the EDC Clinical Trial Designer will ensure that all relevant standard operating procedures, CRF Standards, process and trial-specific guidelines are implemented and utilized to help ensure that a quality work product is produced and timelines and deliverables are consistently met.Summary of the Essential Functions ...

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 ...