2 of 2 Remote/Hybrid Good Clinical Practice Jobs in Sussex

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 ...