
Data-Driven Clinical Trials Expert
2 weeks ago
This role is responsible for leading the statistical programming efforts in the development of clinical trials data.
- Drive innovation and collaboration to deliver high-quality results under tight timelines.
The ideal candidate will have strong expertise in SAS programming, Efficacy analysis, and CDISC standards.
Responsibilities:- Perform advanced data manipulation, analysis, and reporting using SAS programming.
- Develop and validate complex datasets/analysis files, tables, listings, and figures.
- Create detailed reports and documentation utilizing raw data.
- Collaborate with cross-functional teams and clients to ensure project specifications are met.
- Lead duties when called upon and serve as a team player.
- Bachelor's degree in Statistics, Computer Science, or related field.
- At least 7 years of SAS programming experience working with clinical trial data.
- Strong understanding/experience of Efficacy analysis.
- Proficiency in CDISC SDTM / ADaM standards.
- Excellent analytical and troubleshooting skills.
- Ability to provide quality output and deliverables in adherence with challenging timelines.
We believe in applying scientific rigor to reveal the full promise inherent in data, nurturing intellectual curiosity, and inviting a diversity of perspectives to create a wealth of possibilities.
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