About this opportunity
Cytel lists this Senior Statistical Programmer Lead — CDISC & Submissions opportunity in dover, Delaware. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Cytel Inc. is seeking a Principal Statistical Programmer to work embedded with a major pharmaceutical client. You will lead SAS programming for complex clinical trial analyses and support regulatory submissions with minimal supervision.
Qualifications include an MS or BS in biostatistics with 8+ or 10+ years in pharma, expert SDTM/ADaM knowledge, Define.xml review, and strong communication. This role offers independent ownership and collaboration across CROs, FDA interactions, and internal teams.
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Worksite address
dover, DE, 19904, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.