Associate Director, Statistical Programming — Remote

Travere Therapeutics

Detroit (MI)

Hybrid

USD 150,000 - 195,000

Full time

14 days+

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Job summary

Travere Therapeutics in San Diego, CA is seeking an Associate Director of Statistical Programming to provide hands-on programming support across programs, lead external vendors, and ensure timely, high-quality deliverables. The role requires 8+ years SAS programming in clinical trials, 3-5 years of leadership as Lead Programmer, and strong SDTM/ADaM and regulatory expertise. Collaboration with Biometrics and cross-functional teams is essential.

Qualifications

  • Bachelor's degree in Statistics, Computer Science, Mathematics, or related discipline; Masters preferred.
  • Minimum 8 years' clinical research SAS programming in pharmaceutical/CRO environment.
  • 3-5 years progressive leadership with at least 3 years as Lead Programmer.

Responsibilities

  • Provide strategic input on developing programming processes and maintain SOPs, work instructions, and technical standards.
  • Develop programming standards and tools to improve efficiency for analysis and reporting in clinical development projects.
  • Lead projects and oversee contractors to ensure quality and timely programming deliverables.
  • Program analysis datasets, tables, figures, listings, and submission-related outputs (ISS, ISE, DSUR, PSUR, IB, etc.).
  • Review/Develop CDISC specifications and define SDTM/ADaM data sets and Define.xml with supporting documentation.

Skills

SAS programming
Leadership experience
Cross-functional collaboration
Regulatory knowledge
Project management

Education

Bachelor's degree in Statistics/CS/Math
Masters preferred

Tools

SAS (ODS, SQL, MACRO, GRAPH)
UNIX
Windows
MS Office
R (plus)

Job description

Travere Therapeutics in San Diego, CA is seeking an Associate Director of Statistical Programming to provide hands-on programming support across programs, lead external vendors, and ensure timely, high-quality deliverables. The role requires 8+ years SAS programming in clinical trials, 3-5 years of leadership as Lead Programmer, and strong SDTM/ADaM and regulatory expertise. Collaboration with Biometrics and cross-functional teams is essential.
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