Remote Associate Director, Statistical Programming

Travere Therapeutics

Providence (RI)

On-site

USD 150,000 - 195,000

Full time

14 days+

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Job summary

Travere Therapeutics is seeking an Associate Director, Statistical Programming to lead programming across programs and support regulatory submissions. The candidate will oversee external vendors, drive standardization of programming practices, and provide technical leadership within Biometrics.

The role requires strong SAS skills, CRO/vendor management, and deep knowledge of CDISC standards, SDTM/ADaM, and regulatory expectations.

Qualifications

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

Responsibilities

Provide strategic input on programming processes and SOPs; maintain technical standards.
Develop tools to improve efficiency for clinical development analysis and reporting.
Lead projects, oversee contractors, ensure quality and timeliness of deliverables.
Program analysis datasets, tables, figures, listings, and regulatory submission materials.
Review CDISC specifications and define SDTM/ADaM datasets and Define.xml.
Provide programming support for study reports and coordinate with CROs and Biometrics team.
Develop/review SAPs, CRFs, and validation plans; ensure compliance.