Remote Senior Statistical Programmer – SAS & CDISC Expert

Cytel; Augusta (ME); On-site; USD 110,000 - 160,000; Full time

Job summary

Cytel is seeking a Senior Statistical Programmer focused on SAS programming and CDISC SDTM/ADaM to support one or more clinical trials worldwide; role can be fully remote.

You will lead data manipulation, generate TLFs, contribute to submissions, and work with cross-functional teams. Requires 8+ years SAS in pharma/biotech; SDTM/ADaM expertise; study lead preferred; strong QC and analytics.

Qualifications

• 8+ years SAS programming in pharma/biotech with a bachelor’s degree.
• Master’s degree or higher preferred with study lead experience.
• Strong SAS data manipulation, analysis and reporting skills.
• Solid experience implementing the latest CDISC SDTM/ADaM standards.
• Excellent QC/validation capabilities and problem solving.
• Ability to deliver under tight timelines and collaborate globally.
• Experience supporting submissions and eCTD/documentation is a plus.
• Immunology/respiratory/oncology study exposure is beneficial.

Responsibilities

• Perform data manipulation, analysis and reporting of clinical trial data (safety and efficacy).
• Generate and validate SDTM/ADaM datasets and TLFs.
• Production and QC/validation programming.
• Create complex ad-hoc reports from raw data.
• Apply strong efficacy analysis expertise.
• Prepare submission documents and eCRTs.
• Collaborate with cross-functional teams and clients on specs and status.
• Lead when called upon and support team goals.
• Adapt to changing priorities while meeting deadlines.

Skills

SAS programming

Data manipulation

Efficacy analysis

Ad-hoc reporting

QC/Validation

Lead duties

Cross-functional teamwork

Education

Bachelor's degree in Statistics/Computer Science/Mathematics

Master's degree or above

Tools

SAS

CDISC SDTM

CDISC ADaM

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Job description

Cytel is seeking a Senior Statistical Programmer focused on SAS programming and CDISC SDTM/ADaM to support one or more clinical trials worldwide; role can be fully remote.

You will lead data manipulation, generate TLFs, contribute to submissions, and work with cross-functional teams. Requires 8+ years SAS in pharma/biotech; SDTM/ADaM expertise; study lead preferred; strong QC and analytics.