Full Job Description

Role Overview As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. You will be working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you. What You Will Do Performing data manipulation, analysis and reporting of clinical trial data, generating and validating SDTM and ADaM datasets/analysis files, and creating and reviewing submission documents and eCRTs. Why It Might Be a Fit We believe in applying scientific rigor to reveal the full promise inherent in data, and we prize innovation and seek intelligent solutions using leading-edge technology. Requirements Advanced SAS programming skills Proficiency in CDISC standards (SDTM & ADaM) Strong understanding/experience of Efficacy analysis Ability to communicate with and/or respond to internal cross-functional teams and client

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