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3 days ago
Cytel is a leader in delivering high-quality clinical trials, and we're looking for an experienced Senior Statistical Programmer to join our team.
As part of our global pharmaceutical client, you'll be at the heart of their innovation, working on Phase I-IV clinical trials. Our ideal candidate has advanced SAS programming skills, proficiency in CDISC standards (SDTM & ADaM), and experience working with clinical trial data in the Pharmaceutical & Biotech industry.
We value intellectual curiosity, collaboration, and innovation, and are seeking someone who shares these values.
Responsibilities:- Performing data manipulation, analysis and reporting of clinical trial data, utilizing SAS programming.
- Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
- Production and QC/validation programming.
- Generating complex ad-hoc reports utilizing raw data.
- Applying strong understanding/experience of Efficacy analysis.
- Creating and reviewing submission documents and eCRTs.
- Communicating with internal cross-functional teams and clients for project specifications, status, issues or inquiries.
- Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- At least 7 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent.
- Study lead experience, preferably juggling multiple projects simultaneously.
- Strong SAS data manipulation, analysis and reporting skills.
- Solid experience implementing the latest CDISC SDTM / ADaM standards.
- Strong QC/validation skills.
- Good ad-hoc reporting skills.
- Proficiency in Efficacy analysis.
We offer consistent training, development and support to enable our employees' success. If you have a passion for statistical programming and a drive to deliver high-quality results, we encourage you to apply.
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