via Indeed
$90K - 130K a year
Provide statistical programming support for clinical trials including dataset development, reporting, and oversight of CRO programming tasks.
Master's degree with 5 years or bachelor's with 7 years experience in statistical programming using SAS and clinical trial data standards.
Overview Priovant is committed to developing therapies that address high unmet need in autoimmune disease. The Principal/Associate Director Statistical Programmer will help advance this mission by providing programming support across therapeutic areas and in all phases of clinical development. S/he will report to the Director of Statistical Programming in the Biometrics department. Responsibilities • Provide programming support for the clinical trials as assigned that includes but not limited to: • Review of case report forms and EDC for data integrity • Development of SDTM and ADaM datasets, specifications and CDISC components from completed and ongoing studies • Development and execution of blinded dry run and reporting tables, listings and figures • Review of analysis plans from a programmer's perspective • Review of IDMC output and algorithms, where needed • Ad-hoc support for study teams that includes production and validation for internal needs • Programming support for DSURs, Integrated Safety Summaries, patient profiles, etc. • Ensure accurate and compete TMF, for inspection readiness • Rapid turn-around for regulatory request for information (RFIs) • Provide oversight (as needed) of Statistical Programming from CROs by ensuring the programming tasks are completed and delivered in accordance with timelines and data quality standards Qualifications • Master's degree in computer science, biostatistics or related field with 5 years of experience or bachelor's degree with 7 years relevant experience • Expert knowledge in SAS (SAS/BASE, SAS/STAT, SAS/GRAPH, SAS/MACRO, SAS/ODS) • Advance knowledge and experience with SDTM Implementation and ADaM implementation according to CDISC Standards • Knowledge of statistics procedures within SAS/STAT and experience leading a phase 2 or phase 3 study reporting effort from database build to study read-out and archival. • Organized and thorough with very high attention to details • Hands-on, roll-up-your-sleeves approach, with a high sense of urgency and drive for results • Demonstrated excellent communication (written and verbal), problem-solving, and decision-making skills • Natural collaborator who enjoys working on a cross-functional team
This job posting was last updated on 12/3/2025