Senior Manager, Statistical Programming — Remote Impact

Travere Therapeutics; Columbus (OH); Hybrid; USD 132,000 - 172,000; Full time

Benefits offered by this job

Premium health benefits

Retirement plans with company match

Generous paid time off

Job summary

Travere Therapeutics is seeking a Senior Manager, Statistical Programming to provide programming support across all programs within Biometrics. The role includes independent planning, hands-on programming, validation, and vendor oversight to ensure timely, high-quality deliverables.

Responsibilities include developing standards, leading projects, and supporting regulatory submissions with SDTM/ADaM expertise. Strong SAS and CDISC experience are essential, with international travel up to 10%.

Qualifications

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

Responsibilities

• Provide strategic input on statistical programming processes and SOPs.
• Develop programming standards and tools to improve efficiency and accuracy for clinical projects.
• Lead projects, oversee contractors, and ensure timely, quality programming deliverables.
• Program analyses datasets, tables, figures, listings, ISS/ISE, DSUR/PSUR/IB, and submissions.
• Review CDISC specs and generate SDTM/ADaM datasets and Define.xml with documentation.
• Provide SAPs, CRFs, DB specs, validation plans, and reporting datasets; support regulatory submissions.

Skills

SAS programming

CDISC (SDTM/ADaM)

Regulatory submissions

Leadership/lead programmer

UNIX/Windows

SQL/MACRO

Education

Bachelor's degree in Statistics/CS/Math

Master's degree preferred

Tools

SAS

R

SQL

Job description

Travere Therapeutics is seeking a Senior Manager, Statistical Programming to provide programming support across all programs within Biometrics. The role includes independent planning, hands-on programming, validation, and vendor oversight to ensure timely, high-quality deliverables.

Responsibilities include developing standards, leading projects, and supporting regulatory submissions with SDTM/ADaM expertise. Strong SAS and CDISC experience are essential, with international travel up to 10%.