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Open nowPosted 4227 days ago

Clinical Data Analyst

Integrated Resources INC2,463 open roles

Where
Jersey City, NJ, United States
Work mode
On site
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Your applicationOpen nowClinical Data AnalystIntegrated Resources INC · Jersey City, NJ, United States

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. Integrated Resources INC postings stay open a median of 15 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.7%14 days
  5. 35.6%30 days
  6. 58.0%60 days
This job: posted 4227 days ago

Integrated Resources INC median: 15 days open

The posting

Company Description

A 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 Description

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)

Additional Information

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

https://www.linkedin.com/nhome/?trk=nav_responsive_tab_home

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