Summary:ย
Responsible for setting up clinical trials in the iDARTs application, an internally developed tool for medical review of clinical trial data based on TIBCO's Spotfire.ย
At the trial level, perform the following activities:ย
Analysis, design and data mapping of new trials for iDartsย
At the Therapeutic Area level:ย
Contribute to the further improvement of our template libraryย
Function as daily liaison between Clinical team members and the iDarts development and implementation team
Responsibilities :
Analysis and design of iDarts for new studiesย
Design visualizations in line with study protocol specifications and translate them to specificationsย
Data mapping of iDarts for new studiesย
Map iDarts data visualizations to the clinical trial database. SDTM knowledge is a big asset.ย
User Acceptance Testing of iDartsย
Test new study set-up in iDarts before release in to productionย
Team responsibilities for iDarts implementation
Help ensure that all new studies are set-up in iDarts on time.ย
Provide feedback where needed if questions arise during iDarts set-up
Function as liaison between Clinical team members and the iDarts development and implementation teamย
Identify additional needs for medical review, currently not supported by iDartsย
Provide input to the iDarts IT groupย
Follow-up on needed improvements and changes neededย
EDUCATION & EXPERIENCE REQUIREMENTS:ย
BS/BA degree or professional experience equivalentย
Good knowledge of TIBCO Spitfireย
Minimum of 3 to 5 years of pharmaceutical or health care experience, including data analysis.ย
Good understanding of Clinical trials (including database structures & design)ย
Regards,
Sweta Verma
IT Recruiter
Integrated Resources, Inc.
ย "INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (7th Year in a Row)
Direct:- 732 549 5907ย
Tel: (732) 549 2030 x 210
Fax: (732) 549 5549
sweta(at)irionline.com
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