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2 days ago
Leverage your expertise in advanced SAS programming and proficiency in CDISC standards to support or lead Phase I-IV clinical trials. This is an exciting opportunity to drive innovation and patient treatment.
Job Responsibilities- Perform data manipulation, analysis, and reporting for clinical trial data, utilizing SAS programming.
- Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and figures.
- Produce high-quality QC/validation programming.
- Generate complex ad-hoc reports from raw data.
- Apply a strong understanding of efficacy analysis.
- Create and review submission documents and eCRTs.
- Communicate with internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
- Lead duties when called upon.
- A Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- At least 7 years of SAS programming experience with clinical trial data in the pharmaceutical industry.
- Study lead experience, preferably juggling multiple projects simultaneously.
- Strong SAS data manipulation, analysis, and reporting skills.
- Solid experience implementing CDISC SDTM / ADaM standards.
- Good QC/validation skills.
- Proficiency in efficacy analysis.
- Familiarity with drug development life cycles and experience manipulating, analyzing, and reporting clinical trials' data.
- Submissions experience using define.xml and other submission documents.
- Experience supporting immunology, respiratory, or oncology studies would be beneficial.
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