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Priovant Therapeutics

Priovant Therapeutics

via Indeed

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Principal/Associate Director, Statistical Programmer

Anywhere
Full-time
Posted 12/2/2025
Verified Source
Key Skills:
SAS programming
SDTM and ADaM datasets
CDISC standards
clinical trial data management
statistical programming

Compensation

Salary Range

$90K - 130K a year

Responsibilities

Provide statistical programming support for clinical trials including dataset development, reporting, and oversight of CRO programming tasks.

Requirements

Master's degree with 5 years or bachelor's with 7 years experience in statistical programming using SAS and clinical trial data standards.

Full Description

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

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