Senior Associate Director, Statistical Programming (Remote)

Travere Therapeutics; Wichita (KS); On-site; USD 150,000 - 195,000; Full time

Job summary

Travere Therapeutics is seeking an Associate Director, Statistical Programming to provide hands-on programming support across multiple clinical programs. You will guide external vendors, ensure timely, high-quality deliverables, and contribute to development standards.

The role requires 8+ years of SAS programming in clinical research, strong leadership, and expertise in SDTM/ADaM, Define.XML, and regulatory submissions. Onsite in San Diego with a collaborative, cross-functional team culture.

Qualifications

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

Responsibilities

• Provides strategic input on programming processes and SOPs.
• Develops programming standards and tools to improve efficiency for analyses and reporting in clinical development.
• Lead projects, oversee contractors, ensure quality and timely programming deliverables.
• Program analysis datasets, tables, figures, listings, ISS/ISE, DSUR, PSUR, IB, progress reports and submissions.
• Reviews/Develops CDISC specifications and Define.xml; creates SDTM/ADaM datasets.
• Provides programming support for study reports and coordinates activities with Biometrics lead and data managers.
• Develops SAPs, CRFs, DB specs, validation plans, TLFs and datasets specifications.
• Applies programming methodologies to support clinical development.

Skills

Leadership

Communication

Project management

Attention to detail

Education

Bachelor's degree in Statistics/Computer Science/Mathematics

Master's degree preferred

Tools

SAS

UNIX

Windows

SDTM

ADaM

Define.XML

R

MS Office

SQL

MACRO

ODS

GRAPH

ACCESS

Job description

Travere Therapeutics is seeking an Associate Director, Statistical Programming to provide hands-on programming support across multiple clinical programs. You will guide external vendors, ensure timely, high-quality deliverables, and contribute to development standards.

The role requires 8+ years of SAS programming in clinical research, strong leadership, and expertise in SDTM/ADaM, Define.XML, and regulatory submissions. Onsite in San Diego with a collaborative, cross-functional team culture.