4 of 4 Permanent Good Clinical Practice Jobs in Oxford

lifecycle, research ethics and regulatory approval process and the research regulatory frameworks including Research Governance Framework and Good Clinical Practice (ICH-GCP) Main duties of the job The post holder will be the primary contact for providing support and guidance in all aspects relating to data protection … within Good Clinical Practice and adherence to study protocols Desirable Experience of working to ICH Good Clinical Practice (GCP) Knowledge of policy developments in NHS R&D with particular reference to mental and community health care Technical Expertise and Competence Essential Experience with Research ...

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 ...

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 ...