Principal/Associate Director, Statistical Programming - Priovant Therapeutics

Principal/Associate Director, Statistical Programming

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 oversight of Statistical Programming from CROs by ensuring the programming tasks are completed and delivered in accordance with timelines and data quality standards
• Provide programming support for the clinical trials as assigned that includes but not limited to:
  • Review of datasets and CDISC components from completed and ongoing studies
  • Review of blinded dry run outputs that includes confirming derivations of efficacy and safety endpoints
  • 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 and Integrated Safety Summaries
• Maintain up-to-date knowledge of Statistical Programming requirements

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 and the clinical drug development process
• Organized and thorough with attention to details
• Hands-on, roll-up-your-sleeves approach, with a high sense of urgency and drive for results
• Demonstrated excellent communication, problem-solving, and decision-making skills
• Natural collaborator who enjoys working on a cross-functional team

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