Lead Statistical Programmer Clinical Trials Submissions
Listed on 2026-10-15
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IT/Tech
Information Security & Data Protection, Data Analyst, Data Engineering, Data Scientist
Cytel seeks a Principal Statistical Programmer to work embedded with a pharmaceutical client, leading SAS programming for complex trials and regulatory submissions. The role emphasizes independence, project leadership, and collaboration with FDA/ICH regulators. Strong CDISC expertise and Define.xml experience are required.
The position involves working with cross-functional teams to ensure compliant data analysis and timely submissions, with Cytel providing ongoing training and support.
This role, Lead Statistical Programmer for Clinical Trials Submissions at Cytel, could be your next opportunity.
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This posting is for the Lead Statistical Programmer for Clinical Trials Submissions role at Cytel, based in Santa Fe, NM, United States.
We are looking to fill the Lead Statistical Programmer for Clinical Trials Submissions position at Cytel in Santa Fe, NM, United States.
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