|Roles & Responsibilities
|Providing programming expertise in support of the clinical development process. Developing SAS programs to monitor, analyze, and report clinical trial data and managing programming activities and deliverables for contract programmers and external vendors. Acts as a liaison between data management, biostatistics, and clinical operations. Develop SAS programs to analyze and report clinical trial data for CSRs, annual reports, regulatory submissions and publications with a focus on accuracy, completeness, quality, and timely delivery. Manage programming activities and deliverables for contract SAS programmers and external vendors. Ensuring programming is conducted according to departmental and industry standards. Develop and maintain standard SAS macros, templates, and programming standards for biometrics department. Develop and maintain CDISC-compliant SDTM and ADaM data set specifications for clinical studies. Work under supervision. Travel and/or relocation to unanticipated client sites throughout USA is required.