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.