Lead Statistical Programmer - CNS Trials (Remote)

Katalyst CRO; Boulder (CO); Remote; USD 120,000 - 180,000; Part time

Job summary

A leading CRO in the pharmaceutical sector is seeking a skilled statistical programmer for a mid-senior level role. The candidate will lead the development of CDISC-compliant datasets for CNS clinical trials, ensure accuracy of programming deliverables, and mentor junior team members. A bachelor's or master's degree in a relevant field and over 5 years of experience in statistical programming are required. This is a contract position based in Colorado, offering a fully remote setup.

Qualifications

• 5+ years of statistical programming experience in the pharmaceutical, biotech, or CRO industry.
• Experience leading programming efforts for clinical trials, including TLF production and QC oversight.
• Advanced proficiency in SAS using CDISC SDTM and ADaM standards.

Responsibilities

• Lead development of CDISC-compliant datasets for CNS clinical trials.
• Program and QC tables, listings, and figures for clinical study reports.
• Mentor junior programmers and contribute to process improvement.

Skills

SAS proficiency

Statistical programming

Data analysis

Problem-solving

Team collaboration

Attention to detail

Education

Bachelor's or master's degree in Statistics, Biostatistics, Computer Science, Mathematics, or related

Tools

R

Python

Job description

A leading CRO in the pharmaceutical sector is seeking a skilled statistical programmer for a mid-senior level role. The candidate will lead the development of CDISC-compliant datasets for CNS clinical trials, ensure accuracy of programming deliverables, and mentor junior team members. A bachelor's or master's degree in a relevant field and over 5 years of experience in statistical programming are required. This is a contract position based in Colorado, offering a fully remote setup.