Senior Statistical Programming Lead – Remote

Travere Therapeutics; United States; Hybrid; USD 150,000 - 195,000; Full time

Benefits offered by this job

Premium health benefits

Retirement match

Paid time off

Well-being programs

Job summary

Travere Therapeutics is seeking an Associate Director, Statistical Programming in San Diego with remote flexibility. The role involves hands-on SAS programming, leading a biometrics team, and overseeing external vendors to ensure timely deliverables across Phase I–IV trials.

Candidates should have 8+ years in clinical research, strong SDTM/ADaM and Define.XML knowledge, and demonstrated leadership. Collaboration with cross-functional teams and strict adherence to regulatory guidelines are

Qualifications

• Bachelor’s degree in Statistics, Computer Science, Mathematics or related technical discipline; MSc preferred.
• Minimum 8 years’ experience in clinical research, SAS programming for Phase I–IV in pharma/CRO.
• 3–5 years of progressive leadership with at least 3 years as Lead Programmer.

Responsibilities

• Provide hands-on programming and validation support to project teams.
• Oversee external vendors to ensure timely, accurate deliverables.
• Develop programming standards and procedures; work cross-functionally.
• Support submissions and regulatory activities.

Skills

SAS programming

SDTM/ADaM/Define.XML

CDISC/CDASH/eCTD

UNIX/Windows

R Software

MS Office

Project management

Communication

Vendor management

Education

Bachelor’s degree in Statistics, Computer Science, Mathematics

Master’s degree preferred

Tools

SAS

R

SQL

MACRO/GRAPH/ODS

Job description

Travere Therapeutics is seeking an Associate Director, Statistical Programming in San Diego with remote flexibility. The role involves hands-on SAS programming, leading a biometrics team, and overseeing external vendors to ensure timely deliverables across Phase I–IV trials.

Candidates should have 8+ years in clinical research, strong SDTM/ADaM and Define.XML knowledge, and demonstrated leadership. Collaboration with cross-functional teams and strict adherence to regulatory guidelines are