Sign upLog in

Clinical Data Analyst

Integrated Resources, Inc

Jersey City, New Jersey

Apply
JOB DETAILS
JOB TYPE
Full-time
SKILLS
Acceptance Testing, Analysis Skills, Biotech and Pharmaceutical, Clinical Assessment, Clinical Data, Clinical Research, Clinical Trial, Data Analysis, Data Mapping, Data Visualization, Database Design, Healthcare, Information Technology & Information Systems, Rehabilitation Nursing, Research Protocols, TIBCO Product family, Tibco Spotfire, Time Management
LOCATION
Jersey City, New Jersey
POSTED
1 day ago
Clinical Data AnalystA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionSummary: 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 iDartsAt the Therapeutic Area level:Contribute to the further improvement of our template libraryFunction as daily liaison between Clinical team members and the iDarts development and implementation teamResponsibilities :Analysis and design of iDarts for new studiesDesign visualizations in line with study protocol specifications and translate them to specificationsData mapping of iDarts for new studiesMap iDarts data visualizations to the clinical trial database. SDTM knowledge is a big asset.User Acceptance Testing of iDartsTest new study set-up in iDarts before release in to productionTeam responsibilities for iDarts implementationHelp ensure that all new studies are set-up in iDarts on time.Provide feedback where needed if questions arise during iDarts set-upFunction as liaison between Clinical team members and the iDarts development and implementation teamIdentify additional needs for medical review, currently not supported by iDartsProvide input to the iDarts IT groupFollow-up on needed improvements and changes neededEDUCATION & EXPERIENCE REQUIREMENTS:BS/BA degree or professional experience equivalentGood knowledge of TIBCO SpitfireMinimum of 3 to 5 years of pharmaceutical or health care experience, including data analysis.Good understanding of Clinical trials (including database structures & design)

About the Company

I

Integrated Resources, Inc