Remote Senior Manager, Statistical Programming

Travere Therapeutics

San Diego (CA)

On-site

USD 132,000 - 172,000

Full time

3 days ago
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Job summary

Travere Therapeutics in San Diego is seeking a Senior Manager, Statistical Programming to lead programming across clinical programs and ensure timely, high-quality deliverables. You will plan, code, and validate analyses and reports, while guiding CROs and cross-functional teams.

Requirements include 7+ years in clinical research as a SAS programmer, lead programming experience, SDTM/ADaM/Define.XML expertise, and strong communication. On-site with occasional travel; base in San Diego.

Qualifications

  • Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related technical discipline.
  • Master’s degree preferred.
  • 7+ years’ experience in clinical research, ideally as a SAS programmer for phase I–IV trials.
  • Lead Programmer experience is required.
  • Strong knowledge of SDTM, ADaM, Define.XML and regulatory standards.

Responsibilities

  • Provide programming support across all programs and coordinate with Biometrics teams.
  • Lead projects, oversee vendors, and ensure timely, quality programming deliverables.
  • Develop/validate SDTM/ADaM datasets, Define.xml, tables, listings, and figures.
  • Prepare submission programming deliverables and support regulatory filings.
  • Develop SAPs, CRFs, specifications, validation plans, and CSRs; collaborate cross-functionally.

Skills

SAS programming
Lead Programmer
CDISC SDTM/ADaM
Define.XML
Validation
Vendor management
Regulatory submissions
R software
UNIX/Windows
ODS/SQL/MACRO

Education

Bachelor’s degree in Statistics, CS, Math, or related field
Master’s degree preferred

Tools

SAS
R
MS Office
UNIX

Job description

Travere Therapeutics in San Diego is seeking a Senior Manager, Statistical Programming to lead programming across clinical programs and ensure timely, high-quality deliverables. You will plan, code, and validate analyses and reports, while guiding CROs and cross-functional teams.

Requirements include 7+ years in clinical research as a SAS programmer, lead programming experience, SDTM/ADaM/Define.XML expertise, and strong communication. On-site with occasional travel; base in San Diego.

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