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