Senior SAS Clinical Statistical Programmer (CDISC)

TruMinds Clinical; United States; On-site; USD 100,000 - 130,000; Full time

Job summary

A clinical research organization is seeking a highly skilled Senior Statistical Programmer to join their Biometrics team. The ideal candidate will provide programming support for clinical trial data analysis and reporting, ensuring compliance with regulatory standards. Responsibilities include developing SAS programs, collaborating with clinical teams, and mentoring junior programmers. A Bachelor's or Master's degree and extensive experience in the industry are required. This is a full-time role suitable for a mid-senior level professional.

Qualifications

• 9+ years of experience as a Statistical Programmer in the pharmaceutical industry.
• Strong knowledge of CDISC SDTM and ADaM standards.
• Experience with regulatory submissions (FDA, EMA, PMDA).

Responsibilities

• Develop, validate, and maintain SAS programs for clinical trial submissions.
• Ensure programming deliverables are compliant with regulatory guidelines.
• Mentor junior programmers and review their work for quality.

Skills

SAS programming

Communication

Problem-solving

Teamwork

Education

Bachelor’s or Master’s degree in Statistics or related field

Tools

SAS

R

eCTD submissions

Data visualization tools

Job description

A clinical research organization is seeking a highly skilled Senior Statistical Programmer to join their Biometrics team. The ideal candidate will provide programming support for clinical trial data analysis and reporting, ensuring compliance with regulatory standards. Responsibilities include developing SAS programs, collaborating with clinical teams, and mentoring junior programmers. A Bachelor's or Master's degree and extensive experience in the industry are required. This is a full-time role suitable for a mid-senior level professional.