Clinical Trial Database Analyst (SPOTFIRE)

Confidential Company  •  Princeton, NJ
Salary depends on experience
Posted on 08/17/17 by Peter Chen
Confidential Company
Princeton, NJ
Salary depends on experience
Posted on 08/17/17 Peter Chen

Title: Clinical Trial Database Analyst (SPOTFIRE)

Duration: 12-24 months


  • Responsible for visualizing clinical trial data in SPOTFIRE for the Analytical Risk-based Monitoring (ARBM) group 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).


  • Visualizations for ARBM Group:
  • 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%


  • 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.


  • 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)


  • Minimum of a BS/BA degree or professional experience equivalent
  • Advanced knowledge of TIBCO Spotfire required
  • Experience in working with clinical data (plus a general understanding of clinical trials)
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