16 of 16 Remote/Hybrid Clinical Data Management Jobs in the UK

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics … medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s Corporate headquarters are located ...

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 ...

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 ...

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 ...

progress your career. This is a permanent, full-time home-based role in Romania, Bulgaria, Poland, Czech Republic, Hungary.In a client-facing and project management focused role, you will lead eCRF design within the scope of assigned projects. We are looking for an experienced and certified RAVE database designer … specifications for assigned projects to ensure quality and consistencyFollow attention to detail approach and participate in sponsor meetings and audits/inspectionsAssist Managers in data collection for productivity, Quality, timelines and resource planningResponsible for performing quality control procedures for specification developmentConducts team meetings and provide guidance to Programmers ...

with the potential of a salaried position in the future. The Role in 20 Seconds You’ve spent several years working in and around clinical trial systems - EDC, IRT, CTMS, eTMF, ePRO, safety databases - either as a validation specialist, a quality lead, or the person a clinical operations … team calls when a system needs to be inspection-ready. You know GCP well enough to spot the difference between a genuine data integrity risk and a paperwork exercise. You know how to walk into a clinical-stage biotech on a Monday morning, pick up a work package ...

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 ...

recognised specialist biometrics CRO. With more than 30 years of experience and a team of over 150 experts, the organisation provides biostatistics, statistical programming, clinical data management and medical writing services to pharmaceutical, biotechnology and medical-device companies worldwide. This is an excellent opportunity to join … collaborative, technically focused organisation where statisticians work closely with programmers and Data Management teams. You will have direct client contact, influence study design and provide strategic statistical input across a varied portfolio of clinical development programmes. Key Responsibilities Lead statistical activities from study design through to final ...

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 ...