23 of 23 Permanent Clinical Data Management Jobs in England

summary The postholder will translate study protocols and research questions into practical, proportionate data-collection requirements, including the design and refinement of study-specific Case Report Forms (CRFs), database modules, worksheets, data management plans and completion guidance. They will work closely with participating haemophilia centres to facilitate … data collection, resolve operational difficulties and ensure that study data are complete, timely, consistent and suitable for analysis and reporting. The role has three core components: Study-specific data management: Developing and maintaining the additional data-collection tools and processes required for post-marketing ...

Title: Senior Clinical Research Data Manager Location: Salford Quays Salary: £49,387- £56,515 per annum - Band 7 Contract: Full time, Permanent About the Role: The National Haemophilia Database (NHD) is the UK's national registry for people with inherited and acquired bleeding disorders, collecting clinical and treatment data from NHS haemophilia centres across the UK. We are seeking an experienced Senior Clinical Research Data Manager to provide specialist data management and coordination for post-marketing studies, investigator-initiated studies and other approved research delivered through the NHD. Working with ...

Talentmark are looking for a Senior Manager, Data Management to join a long established and successful global pharmaceutical company. This will be a hybrid role, based at their EU headquarters in Hertforshire. The Role: As Senior Manager, Data Management you will be primarily responsible … direct management of clinical study activities as they relate to data collection and processing from study start up through ongoing oversight to completion. Working in a highly matrixed environment, the successful candidate must have proven ability to effectively manage outsourced vendor activities as well as internal resources. ...

role requires to be on-site in our office in Feltham for 3 days per week. Your role As a senior team member within Clinical Data Management, you will lead the end-to-end data management delivery for assigned global Phase I-IV clinical … trials or a defined study portfolio, with a particular focus on complex oncology, neurology or immunology development. You will set the strategic direction for data collection, cleaning, review, reconciliation, and quality activities, ensuring the accuracy, integrity, completeness, and submission-readiness of clinical trial data. Operating with a high ...

KingdomOverviewAre you ready to take a leadership role within a dynamic life sciences organization? This is an exciting opportunity for a strategic and experienced data management professional to influence the future of clinical data operations. You will have the chance to work on impactful projects, lead … cross-functional teams, and shape data strategies in a challenging, fast-moving environment.About our clientOur client is a diverse life sciences organization dedicated to advancing research and development efforts. They focus on improving patient outcomes through innovative solutions and robust clinical trials. This role plays a vital part ...

Ready to shape the future of clinical data standards and influence the success of global oncology studies An established global clinical research organisation is seeking a Principal Clinical Data Standards Specialist to join its expanding team. This senior position provides the opportunity to influence data standards strategy, promote consistency across clinical development programmes, and support the adoption of industry best practices within a collaborative and innovative environment.In this role, you will provide leadership in the development and application of clinical data standards, support regulatory compliance activities, and act as a trusted ...

Your role Are you excited about developing and managing data and technology solutions that support the development of new medicines? We are looking for a Senior Data Engineer to play a key role in enabling data-driven clinical research and development through validated systems, high-quality … data processes, and modern analytics solutions. Job Description Your role Are you excited about developing and managing data and technology solutions that support the development of new medicines? We are looking for a Senior Data Engineer to play a key role in enabling data-driven clinical ...

transforming the life sciences industry, committed to making a positive impact on its customers, employees, and communities. The Role Veeva's Vault Clinical Data Management System (CDMS) is changing how life sciences companies manage clinical trial data, bringing EDC, coding, and Veeva Data Quality … facing role open to candidates working remotely from the EU or UK. What You’ll Do Act as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to meet their goals, and providing training and mentorship along the way Work with customers to interpret clinical ...

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 ...

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 ...

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 ...

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 ...

number of days per week per Company policy. About our Company : Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading … expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market ...

number of days per week per Company policy. About our Company Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading … expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market ...

stakeholders.Mentor junior programmers and share best practices internally and externally.Collaboration & Execution Support sprint planning and project delivery across studies.Collaborate cross-functionally and manage data access appropriately.Support regulatory interactions and contribute to CoE activities.AccountabilitiesServe as Lead Programmer for complex or multiple studies.Ensure quality, compliance, and efficient execution of programming activities.Make … data-driven decisions and proactively address risks and issues.Why You:Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals:Bachelor’s degree in Statistics, Computer Science, or a related field.Expertise in R programming.6+ years of clinical programing experience5+ years ...

junior programmers and share best practices internally and externally. Collaboration & Execution Support sprint planning and project delivery across studies. Collaborate cross-functionally and manage data access appropriately. Support regulatory interactions and contribute to CoE activities. AccountabilitiesServe as Lead Programmer for complex or multiple studies. Ensure quality, compliance, and efficient … execution of programming activities. Make data-driven decisions and proactively address risks and issues. Why You: Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals: Bachelor's degree in Statistics, Computer Science, or a related field. Expertise in R programming.6+ ...

About our Company: Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating 25 years of ground-breaking technological innovation across more than 36,000 trials and 11 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest … clinical trial data sets in the industry. More than 1 million users trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. Discover more at www.medidata.com. Position Overview We are seeking an experienced, growth-minded Senior ...

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 ...