Director of Statistical Programming
VirtualVocations
To support clinical trials from early-stage through regulatory submission, the full-time Director of Statistical Programming will manage programming activities, oversee vendor deliverables, and collaborate with cross-functional teams in a remote work environment. Key responsibilities Lead statistical programming for clinical studies, ensuring high-quality regulatory-compliant deliverables Oversee the creation and maintenance of programming plans and statistical analysis plans in collaboration with biostatisticians Manage CRO programming activities, providing guidance and quality control for outsourced deliverables Required qualifications Graduate degree in Statistics, Biostatistics, or a closely related field 3-5 years of experience in pharmaceutical/biotech programming in a clinical trial environment Expert level of SAS programming skills; knowledge of additional programming languages (e.g., R, Python) is a plus Advanced knowledge of CDISC standards, including CDASH, SDTM, and ADaM Familiarity with ICH guidelines and regulatory submission requirements
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