Senior Statistical Programming Lead - Remote, SD

Travere Therapeutics; Minneapolis (MN); Presencial; USD 132.000 - 172.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Premium health benefits

Life insurance

Retirement plan with employer match

Generous paid time off

Descripción de la vacante

Travere Therapeutics is seeking a Senior Manager, Statistical Programming in San Diego (onsite with remote options). The role provides programming leadership across clinical programs, oversees external vendors, and ensures submissions meet CDISC standards.

The ideal candidate has 7+ years in clinical research with SAS, SDTM/ADaM knowledge, and strong collaboration across Biometrics. The position emphasizes quality, timelines, and regulatory readiness.

Formación

• Bachelor's degree in Statistics, Computer Science, Mathematics, or related field; Master's preferred.
• 7+ years' experience in clinical research with SAS programming for phase I–IV; Lead Programmer experience required.
• Technical knowledge of SDTM, ADaM, and Define.XML.

Responsabilidades

• Provide programming support across programs and coordinate with Biometrics team.
• Develop and review SAPs, CRFs, and data specifications.
• Lead projects, oversee contractors, ensure timely, quality programming deliverables.
• Program datasets, tables, figures, listings, and submission-ready outputs (ISS/ISE/DSUR/PSUR/IB).
• Review CDISC specifications and Define.xml documentation for submissions.
• Support CDISC submission processes and coordinate with CROs and data managers.

Conocimientos

SAS programming

CDISC standards

UNIX/Windows

Vendor management

SQL/MACRO/GRAPH

R familiarity

Educación

Bachelor's degree in Statistics, CS, Mathematics

Master's degree preferred

Herramientas

SAS

R

Descripción del empleo

Travere Therapeutics is seeking a Senior Manager, Statistical Programming in San Diego (onsite with remote options). The role provides programming leadership across clinical programs, oversees external vendors, and ensures submissions meet CDISC standards.

The ideal candidate has 7+ years in clinical research with SAS, SDTM/ADaM knowledge, and strong collaboration across Biometrics. The position emphasizes quality, timelines, and regulatory readiness.