Senior Manager, Statistical Programming — Remote

Travere Therapeutics; New York (NY); Hybrid; USD 132,000 - 172,000; Full time

Job summary

Travere Therapeutics invites applications for a Senior Manager, Statistical Programming in the Biometrics team. The role collaborates with the Associate Director and project teams to provide programming support across programs, ensuring quality and timely deliverables.

It includes vendor oversight and cross-functional coordination. The ideal candidate will have 7+ years in clinical research with SAS programming for phase I-IV trials, CDISC knowledge, and strong communication skills.

Qualifications

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

Responsibilities

• Provide strategic input on programming processes and maintain SOPs, work instructions, and standards.
• Develop tools to improve efficiency and accuracy for analyses and reporting in clinical development.
• Lead projects, oversee contractors, and ensure quality and timeliness of programming deliverables.
• Program analysis datasets, tables, figures, listings, and regulatory submissions.
• Review CDISC specs and generate SDTM/ADaM data sets and Define.xml with documentation.
• Provide programming support for study reports and coordinate with CROs and Biometrics leads.
• Develop/Review SAPs, CRFs, DB specs, validation plans, and datasets specifications.
• Contribute to applying programming methodologies in clinical development.

Skills

SAS programming

SDTM

ADaM

Define.XML

CDISC standards

Vendors management

Leadership

UNIX/Windows

Regulatory knowledge

Education

Bachelor's degree in Statistics/CS/Math

Master's degree preferred

Tools

SAS

R

Job description

Travere Therapeutics invites applications for a Senior Manager, Statistical Programming in the Biometrics team. The role collaborates with the Associate Director and project teams to provide programming support across programs, ensuring quality and timely deliverables.

It includes vendor oversight and cross-functional coordination. The ideal candidate will have 7+ years in clinical research with SAS programming for phase I-IV trials, CDISC knowledge, and strong communication skills.