1 of 1 Permanent Good Clinical Practice Jobs in Pulborough

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 ...