Job Description
Clinical Trial Database Analyst (SPOTFIRE)
POSITION SUMMARY:
• Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring and for the medical reviewers in the iDARTs application (an internally developed tool for medical review of clinical trial data based on TIBCO’s Spotfire).
PRINCIPAL RESPONSIBILITIES:
• Load/Configure SAS output provided by ARBM programmers in SPOTFIRE template
• Create data visualizations (Tables/Graphs) in SPOTFIRE based on ad-hoc requirements.
• Generate user requirements documentation and setup UAT
• Move visualizations to production through the development stages (dev/qa/prod) per existing process
• Visualizations for Medical Review
• Load the clinical trial datasets (in Study Data Tabulation Model) in Spotfire/iDARTs
• Map existing data visualization templates in iDARTs to the clinical trial datasets
• Collect additional user requirements (from study physicians & data managers) and design new visualizations (Tables/Graphs)
• Design new visualizations (Tables/Graphs) based on the user requirements
• Conduct review sessions with the study team members
• Follow-up on needed improvements and changes needed
• Move visualizations to production through the development stages (dev/qa/prod) per existing process 50%
DECISION-MAKING AND PROBLEM-SOLVING :
• Position requires an open mindset with good issue identification and problem-solving skills. A degree of straightforward decision making is expected, while balancing the need for further escalation of issues that require more complex decisions.
WORKING RELATIONSHIPS/INTERFACES:
• Primarily interacts with
• ARBM team members (SAS Programmers and Central Monitors)
• Clinical study team members (Clinical Scientist, Study Physician, Global Data Manager)
• As needed, interacts with other staff within R&D (eg, biostats & programming