Programming Manager, Clinical Programming

Role: Support clinical trial data standards development and compliance, focusing on SDTM datasets for regulatory submissions within a biopharma setting. Responsibilities: develop and implement SDTM standards aligned with CDISC, review study eCRFs, ensure data quality and regulatory compliance, and support data visualization tools like GenSense Dashboards; contribute to global collaboration and knowledge sharing. Requirements: Bachelor’s in Statistics, Computer Science, or Life Sciences; 3-5 years in pharma, proficiency in SAS, and experience with SDTM data modeling; experience working in a global environment; strong analytical, communication, and organizational skills. Preferred: Master’s degree, additional industry certifications. HighValue: focus on clinical data standards, CDISC compliance, SDTM datasets, and digital solutions for data exchange; role supports global clinical trial operations. Work Setup: flexible work arrangement with 20-40% remote work; no travel specified.