6 of 6 Permanent Good Clinical Practice Jobs in Oxfordshire

Data Transfer Agreements and Data Management Plan drafting. Manage EDC access. Database design, set up, testing and maintenance. Ensure CDM activities conform to ICH GCP guidance. Lead and/or participate in internal and external audits of clinical data management processes. Essential EDC data entry and review. Generating data … Data Transfer Agreements and Data Management Plan drafting. Manage EDC access. Database design, set up, testing and maintenance. Ensure CDM activities conform to ICH GCP guidance. Lead and/or participate in internal and external audits of clinical data management processes. Desirable Assist with Data Transfer Agreements and Data ...

summary The NIHR Oxford Health Clinical Research Facility is seeking a Clinical Research Laboratory and Biostorage Coordinator to support the delivery of a diverse portfolio of research studies and the day-to-day operation of the CRF laboratory and biostorage service. The successful candidate will play … subject, or equivalent relevant knowledge and experience. Evidence of continuing professional development relevant to laboratory, research or biostorage practice. Desirable Relevant specialist training, e.g. Good Clinical Practice, Good Laboratory Practice, biological sample shipping or human tissue governance Experience Essential Significant practical experience in a research ...

requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Responsibilities: Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables … Data Manager and Study Leader. Education and Experience: Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have ...

within the pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience in generating and validating SDTM, ADaM, and TLFs Good understanding of CDISC standards and clinical trial processes Ability to work independently and manage multiple priorities in a fast-paced environment Experience supporting … regulatory submissions is preferred Strong communication and stakeholder management skills Responsibilities: Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Create datasets, tables, listings, and figures according to study requirements Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards ...

industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience supporting regulatory submissions is preferred Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards and project timelines Participate … study planning, review specifications, and support submission activities Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master's degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Working knowledge ...

Perspectum Ltd is seeking a Clinical Data Manager I responsible for ensuring trial data is accurate, complete, and aligns with study protocols and SOPs. You will collaborate with clinical operations, biostatistics and medical writing to support collection, management and analysis of data. You are detail-oriented with … passion for clinical research and data management. The role involves EDC data entry, data queries, database design and participation in quality audits in line with ICH GCP. #J-18808-Ljbffr ...