
Principal Clinical Data Analyst
1 day ago
Job Overview
We are seeking a highly skilled Senior Statistical Programmer to join our team. The ideal candidate will have advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM).
The successful candidate will be responsible for supporting or leading one or more Phase I-IV clinical trials, leveraging their expertise in data manipulation, analysis and reporting of clinical trial data.
About the RoleThis is an exciting opportunity for a motivated and detail-oriented individual to work on complex projects, collaborating with cross-functional teams and clients.
As a Senior Statistical Programmer, you will have the opportunity to grow your career in a dynamic and supportive environment, receiving consistent training, development and support.
Responsibilities- 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
- Efficacy analysis
- Creating and reviewing submission documents and eCRTs
- Bachelor's degree in Statistics, Computer Science, Mathematics or related field
- At least 7 years of SAS programming experience in the Pharmaceutical & Biotech industry
- 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
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