Remote Senior Statistical Programmer - SAS & CDISC

Cytel; San Juan (PR); On-site; USD 110,000 - 170,000; Full time

Job summary

Cytel, a leading provider of biostatistics software and services, seeks a Senior Statistical Programmer to support or lead Phase I–IV clinical trials, using SAS and CDISC SDTM/ADaM standards. This role can be performed fully remote in the United States.

You will perform data manipulation, analysis and reporting; generate SDTM/ADaM datasets and TLFs; contribute to submissions and eCRTs; lead activities when called upon and collaborate with cross‑functional teams to deliver high‑quality results on

Qualifications

• Bachelor’s degree in Statistics, Computer Science, Mathematics or similar.
• At least 8 years SAS programming with clinical trial data; 6+ years with Master’s.
• Strong CDISC SDTM/ADaM experience and submission document familiarity.
• Ability to lead and collaborate across cross-functional teams.

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data using SAS.
• Generate and validate SDTM/ADaM datasets and TLFs; produce submission-ready outputs.
• Conduct production and QC/validation programming; support or lead trials.
• Prepare complex ad-hoc reports and contribute to eCRTs and define.xml.
• Lead duties when called upon and collaborate with global teams.

Skills

SAS programming

CDISC SDTM/ADaM

Data manipulation & reporting

Efficacy analysis

Ad-hoc reporting

QC / validation

Submission documents experience

Lead experience

Team collaboration

Education

Bachelor’s degree in Statistics/Computer Science/Mathematics

Advanced degree (MS/Master’s) preferred

Tools

SAS Software

Job description

Cytel, a leading provider of biostatistics software and services, seeks a Senior Statistical Programmer to support or lead Phase I–IV clinical trials, using SAS and CDISC SDTM/ADaM standards. This role can be performed fully remote in the United States.

You will perform data manipulation, analysis and reporting; generate SDTM/ADaM datasets and TLFs; contribute to submissions and eCRTs; lead activities when called upon and collaborate with cross‑functional teams to deliver high‑quality results on