Senior Manager, Clinical Programming

Role: Senior Manager, Clinical Programming responsible for developing and maintaining SDTM standards to ensure data quality, consistency, and regulatory compliance in clinical trial data management. Responsibilities include creating SDTM standards aligned with CDISC and industry regulations, reviewing study eCRFs, supporting data collection standardization, conducting quality control, and facilitating process improvements. Acts as a subject matter expert on data standards, supports implementation of technology solutions, and liaises with external data management teams to ensure data standardization across programs. Requirements: Bachelor's in Statistics, Computer Science, or Life Sciences; 6-8 years of relevant experience in pharma, biotech, or CRO; proficient in SAS programming; knowledge of industry standards (CDISC), FDA, ICH, GCP; strong project management and communication skills; experience in clinical data management or standards management preferred. HighValue: expertise in SDTM standards development, CDISC compliance, clinical data standards, regulatory submission support, and cross-functional collaboration. WorkSetup: not specified.