Senior Clinical Programmer: Data Management & Compliance

Cytel is seeking a skilled clinical programmer with 4-6 years of experience to manage clinical trial data processes. Responsibilities include writing and maintaining code, ensuring data quality, and collaborating with stakeholders. Candidates should have proficiency in programming languages such as SAS, R, and SQL, alongside a strong understanding of clinical trial data standards. A Bachelor's degree in a related field is required. This role is based in Des Moines, Iowa.
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