Job Description

Clinical Trial Database Analyst (SPOTFIRE) Contract Katalyst 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. Title: Clinical Trial Database Analyst (SPOTFIRE) Duration: 12-24 months

POSITION 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 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)

EDUCATION & EXPERIENCE REQUIREMENTS:

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) All your information will be kept confidential according to EEO guidelines. #J-18808-Ljbffr Katalyst Healthcares & Life Sciences

Job Tags

Contract work, Immediate start,

Similar Jobs