
Senior Data Analyst
3 days ago
Key Responsibilities
As a senior statistical programmer, you will be responsible for the data manipulation, analysis, and reporting of clinical trial data. This includes performing data manipulation, generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs). You will also be required to generate complex ad-hoc reports utilizing raw data.
Requirements
- 7 years of SAS programming experience in the pharmaceutical & biotech industry, with a bachelor's degree or equivalent. Alternatively, 5 years with a master's degree or above.
- Study lead experience, preferably juggling multiple projects simultaneously preferred.
- 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.
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
- Submissions experience utilizing define.xml and other submission documents.
Benefits
- Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
- We believe in applying scientific rigor to reveal the full promise inherent in data.
- We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
- We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
- We prize innovation and seek intelligent solutions using leading-edge technology.
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