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Clinical Database Analyst

Integrated Resources, Inc

Lexington, Massachusetts

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Analysis Skills, Biotech and Pharmaceutical, Clinical Assessment, Clinical Data, Clinical Monitoring, Clinical Research, Clinical Trial, Communication Skills, Computer Programming, Customer Relations, Customer/Client Research, Data Management, Data Modeling, Data Visualization, Database Analysis, Healthcare, Identify Issues, Problem Solving Skills, Product Requirements Document (PRD), Quality Assurance, Research & Development (R&D), Risk Management, Statistical Analysis System (SAS), Tibco Spotfire, Training Data Sets
LOCATION
Lexington, Massachusetts
POSTED
1 day ago
Clinical Database AnalystResponsible 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: % Of Time• Visualizations for ARBM Group:o Load/Configure SAS output provided by ARBM programmers in SPOTFIRE templateo Create data visualizations (Tables/Graphs) in SPOTFIRE based on ad-hoc requirements.o Generate user requirements documentation and setup UATo Move visualizations to production through the development stages (dev/qa/prod) per existing process• Visualizations for Medical Reviewo Load the clinical trial datasets (in Study Data Tabulation Model) in Spotfire/iDARTso Map existing data visualization templates in iDARTs to the clinical trial datasetso Collect additional user requirements (from study physicians & data managers) and design new visualizations (Tables/Graphs)o Design new visualizations (Tables/Graphs) based on the user requirementso Conduct review sessions with the study team memberso Follow-up on needed improvements and changes neededo 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)Education & Experience Requirements:• Minimum of a BS/BA degree or professional experience equivalent• At least 1 year relevant experience in pharmaceutical or health care industry• Advanced knowledge of TIBCO Spotfire required• Experience in working with clinical data (plus a general understanding of clinical trials) strongly preferredQualities and Characteristics:• Communication skills and active listening• Strong customer focus• Strong analytical mindset & Quality oriented• Innovative thinking• Flawless execution

About the Company

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Integrated Resources, Inc