The client is seeking a Senior Clinical Trial Data Analyst to support study teams by delivering timely and high-quality centralized monitoring tools and analysis, including the development and maintenance of reports for study specific Key Risk Indicators (KRIs) and Quality Tolerance Limit parameters (QTLs).
Requirements
- Proficient in data analysis tools (e.g., R, Python, JMP) for manipulating, analyzing large datasets, creating data visualizations (e.g., Tableau, Spotfire), and applying statistical methods (hypothesis testing, regression analysis, data modeling) to analyze clinical trial data
- Experience and understanding of clinical trial data from various sources (e.g. Veeva, RAVE, IRT, SDTM, clinical devices, etc)
- 6+ years' experience in Biotech/Pharmaceutical industry with knowledge of the pharmaceutical/biotech clinical development process
Responsibilities
- delivering timely and high-quality centralized monitoring tools and analysis, including but not limited to the development and maintenance of reports for study specific Key Risk Indicators (KRIs) and Quality Tolerance Limit parameters (QTLs).
- Provide training and knowledge sharing to study teams to promote RBQM analysis solutions and best practices.
- Lead centralized systematic data surveillance across studies in ECD, document surveillance activities, and assess control measure outputs for necessary mitigating actions.
Other
- Senior Clinical Trial Data Analyst
- Biotech/Pharmaceutical industry
- pharmaceutical/biotech clinical development process
