
Senior Statistical Data Analyst
2 days ago
At Cytel, we are driving innovation in patient treatment. We believe in the power of data to reveal new insights and possibilities.
As a Senior Statistical Programmer, you will be at the heart of our client's innovation. You will work fully embedded within one of our global pharmaceutical clients, with the support of our team behind you.
Job Title: Senior Statistical Programmer- Scientific Rigor
- We apply scientific rigor to uncover the full potential in data.
- Collaboration
- We encourage collaboration and invite diverse perspectives to drive discovery.
- Innovation
- We foster innovation and explore intelligent solutions using leading-edge technology.
- Quality
- We prioritize quality and seek excellence in all aspects.
Responsibilities:
How you will contribute:
- Data Analysis
- You will perform data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.
- Reporting
- You will generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
- Communication
- You will communicate with internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
- Leadership
- You will perform lead duties when called upon.
Qualifications:
To succeed in this position, you will have:
- Bachelor Degree
- A bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- Programming Skills
- At least 7 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 5 years of related experience with a master's degree or above.
- Study Lead Experience
- Study lead experience, preferably juggling multiple projects simultaneously.
- Analysis Skills
- Strong SAS data manipulation, analysis, and reporting skills.
- QC Skills
- Solid experience implementing CDISC SDTM / ADaM standards.
- Submission Skills
- Submissions experience utilizing define.xml and other submission documents.
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