10 of 10 CDISC Jobs in London

your role and expand your skills. Beneficial Experience Knowledge of the clinical drug development process and relevant disease areas. Awareness of industry standards and ICH guidelines. Experience working to CDISC Standards. Excellent time-management and self-management skills for competing priorities. Ability to work independently and as part of a collaborative team. If you're passionate about delivering high-quality More ❯

your role and expand your skills. Beneficial Experience Knowledge of the clinical drug development process and relevant disease areas. Awareness of industry standards and ICH guidelines. Experience working to CDISC Standards. Excellent time-management and self-management skills for competing priorities. Ability to work independently and as part of a collaborative team. If you're passionate about delivering high-quality More ❯

your role and expand your skills. Beneficial Experience Knowledge of the clinical drug development process and relevant disease areas. Awareness of industry standards and ICH guidelines. Experience working to CDISC Standards. Excellent time-management and self-management skills for competing priorities. Ability to work independently and as part of a collaborative team. If you're passionate about delivering high-quality More ❯

your role and expand your skills. Beneficial Experience Knowledge of the clinical drug development process and relevant disease areas. Awareness of industry standards and ICH guidelines. Experience working to CDISC Standards. Excellent time-management and self-management skills for competing priorities. Ability to work independently and as part of a collaborative team. If you're passionate about delivering high-quality More ❯

creative thinking, attention to detail and empathy for patients to data management, and use these skills to ensure the highest quality trial outcome Bonus: You have experience working with CDISC standards such as SDTM You belong here! If your experience and interests match with some of the above, we want you to apply. What you'll focus on Become an More ❯

a Subject Matter Expert. In this role you will Analysis and Reporting Standards Development and Management Develop, manage, and optimize GSK-specific data standards, aligning with industry benchmarks (e.g., CDISC), regulatory and scientific requirements to define custom standards, and creating supporting documentation in response to business needs. Cross-Functional Collaboration Lead, coordinate and contribute to cross-functional teams - engaging representatives … processes and technologies related to data standards maintenance and adoption. Leadership and Oversight Provide oversight and guidance to CRO partners, represent the organization in internal and external initiatives (e.g., CDISC, PhUSE), manage matrix teams, and support talent development through coaching, mentoring, appraisals, and workload management. Advocacy and Consultancy Act as a champion for data standards across the organization, supporting stakeholder … experience, in Life Sciences, Computer Sciences, Mathematics and Physics or equivalent. Proven experience working in pharmaceutical industry/Clinical Trial, Clinical Programming with expertise in industry data standards (e.g., CDISC) and deep understanding of analysis and reporting requirements for clinical trials. Proven ability to analyse business problems/opportunities within at least one of the data stewardship areas (e.g., asset More ❯

a Subject Matter Expert. In this role you will Analysis and Reporting Standards Development and Management Develop, manage, and optimize GSK-specific data standards, aligning with industry benchmarks (e.g., CDISC), regulatory and scientific requirements to define custom standards, and creating supporting documentation in response to business needs. Cross-Functional Collaboration Lead, coordinate and contribute to cross-functional teams - engaging representatives … processes and technologies related to data standards maintenance and adoption. Leadership and Oversight Provide oversight and guidance to CRO partners, represent the organization in internal and external initiatives (e.g., CDISC, PhUSE), manage matrix teams, and support talent development through coaching, mentoring, appraisals, and workload management. Advocacy and Consultancy Act as a champion for data standards across the organization, supporting stakeholder … experience, in Life Sciences, Computer Sciences, Mathematics and Physics or equivalent. Proven experience working in pharmaceutical industry/Clinical Trial, Clinical Programming with expertise in industry data standards (e.g., CDISC) and deep understanding of analysis and reporting requirements for clinical trials. Proven ability to analyse business problems/opportunities within at least one of the data stewardship areas (e.g., asset More ❯

Trial Team (CTT). Review eCRF, discuss data structures and participate in data review activities as member of the extended CTT. Comply with company, department and industry standards (e.g. CDISC) and processes, assess and clarify additional programming requirements at project-level, review and develop programming specifications as part of the analysis plans. Provide and implement statistical programming solutions; ensure knowledge … programming deliverables as well as accuracy and reliability of statistical analysis results. Maintain up-to-date advanced knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC SDTM/ADaM, eCTD, Define.xml), attend functional meetings and trainings. Establish successful working relationship on individual studies with external associates according to agreed contract and internal business guidance As assigned … environment to develop and validate deliverables. Plus R. Advanced experience in contributing to statistical analysis plans and/or constructing technical programming specifications Good knowledge of industry standards including CDISC data structures as well as a solid understanding of the development and use of standard programs Good understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, study procedures). More ❯

motivated and friendly team as Statistical Programmer (UK Remote) Your responsibilities You program and validate statistical analysis of clinical studies with SAS. You define and program analysis datasets and CDISC SDTM and ADaM datasets in SAS. You are responsible for the quality control of evaluations of clinical studies. You conduct all other programming activities needed during a clinical study. You … experience in programming activities of clinical studies. You have very good programming skills in SAS 9, experience in R would be a benefit. You have gained practical experience with CDISC SDTM and ADaM standards. You have a degree in medical documentation, mathematical biometrics, statistics, mathematics, computer science or a comparable qualification. You are communicative and carry out the required communication More ❯

involves leading data strategy development, managing timelines and deliverables. The DML ensures data collection tools, data cleaning processes, and database lock procedures are aligned with regulatory requirements (e.g. GCP, CDISC standards) and project goals. They also manage vendors and internal data teams, driving efficiency, accuracy, and innovation in clinical data handling. Key Accountabilities: Lead the development and execution of data … and validation of clinical databases and eCRFs in alignment with study protocols and regulatory standards. Ensure all data management activities comply with GCP, internal SOPs, and industry regulations, including CDISC standards. Manage data cleaning processes, including query generation and resolution, coding, and reconciliation of third-party data sources. Act as the primary point of contact for all data management activities More ❯