Company DescriptionKatalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.Job DescriptionTitle: Clinical Trial Database Analyst (SPOTFIRE)Duration: 12-24 monthsPOSITION SUMMARY: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).PRINCIPAL RESPONSIBILITIES:Visualizations for ARBM Group:Load/Configure SAS output provided by ARBM programmers in SPOTFIRE templateCreate data visualizations (Tables/Graphs) in SPOTFIRE based on ad-hoc requirements.Generate user requirements documentation and setup UATMove visualizations to production through the development stages (dev/qa/prod) per existing processVisualizations for Medical ReviewLoad the clinical trial datasets (in Study Data Tabulation Model) in Spotfire/iDARTsMap existing data visualization templates in iDARTs to the clinical trial datasetsCollect additional user requirements (from study physicians & data managers) and design new visualizations (Tables/Graphs)Design new visualizations (Tables/Graphs) based on the user requirementsConduct review sessions with the study team membersFollow-up on needed improvements and changes neededMove visualizations to production through the development stages (dev/qa/prod) per existing process 50�CISION-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 withARBM 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)EDUCATION & EXPERIENCE REQUIREMENTS :Minimum of a BS/BA degree or professional experience equivalentAdvanced knowledge of TIBCO Spotfire requiredExperience in working with clinical data (plus a general understanding of clinical trials)Additional InformationAll your information will be kept confidential according to EEO guidelines.