Associate Director, Statistical Programming

Role: Associate Director, Statistical Programming supporting clinical development, regulatory submissions, and commercialization of psychedelics-focused therapeutics at different stages. Responsibilities: serve as study lead programmer, review and ensure quality of Define packages (eCRF, SDTM/ADaM datasets, XML), oversee vendor deliverables, perform validation and statistical analysis, collaborate with Data Management, and contribute to analysis plans and regulatory documents. Requirements: Master’s in Biostatistics, Statistics, or related field; 12+ years in clinical trial statistical programming; expertise in CDISC standards, Pinnacle 21, and SAS software; strong project management and collaboration skills; detail-oriented. Preferred: experience with CNS trials and integrated data analysis for regulatory filings. HighValue: late-stage clinical biopharma, psychedelics/neuropsychiatry, regulatory submission support, vendor oversight, CDISC compliance, data analysis, statistical validation. WorkSetup: remote, with a salary range of $155K–$195K USD, plus benefits.