1 of 1 Remote/Hybrid Good Clinical Practice Jobs in Witney

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 ...