9 of 9 Permanent Clinical Data Management Jobs in London

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 ...

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 ...

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 ...

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 ...