Senior Manager, Clinical Programming

To ensure data quality and compliance across clinical programs, the full-time Senior Manager, Clinical Programming will establish SDTM standards, oversee programming activities with vendors, and serve as a subject matter expert on data standards in a remote environment. Key responsibilities Develops and implements SDTM standards ensuring compliance with CDISC and industry regulations Reviews study eCRFs and provides guidance on SDTM mapping to align data collection standards Facilitates continuous improvement of standards processes and serves as a liaison between Clinical Programming and External Data Management Required qualifications Bachelor's degree in Statistics, Computer Science, or Life Sciences; Master's degree preferred 6-8 years of relevant experience in pharmaceutical, biotech, CRO, or regulatory environments Proficient in SAS programming with practical knowledge of R for clinical trials Demonstrated knowledge of clinical research, metadata management, and regulatory requirements Experience managing complex projects and working with cross-functional teams