Job Details

  • Title: Clinical Research Associate
  • Code: RCI-ABT-76876 / 76933
  • Location: Des Plaines Illinois (IL) 60018
  • Posted Date: 04/18/2019
  • Duration: 12 Months
  • Status: Open
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  Job Description

We have 2 different CRA positions with 50% and 35% travel

Travel required ~50%; worker will responsible for initial cost but can be reimbursed w/appropriate receipts for ABLJP00076876 

Travel is required ~35% for ABLJP00076933


3+ Years Experience Level.

Description

  • Member of the clinical team responsible for conducting clinical studies according to Federal Regulations and ICH guidelines
  • This individual will be assigned to one or more projects and will assist with coordination of all study activities including; assisting senior staff in planning study conduct and case report forms (CRFs), Contract Research Organization (CRO) oversight, reagent forecasting and sample accountability, training of investigator sites, monitoring clinical documents, analyzing and evaluating clinical data generated during clinical studies, and assists with assembly of regulatory submission documents
  • Responsible for assisting with basic study protocols, monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary
  • The individual ensures study compliance with protocol, clinical brochure, and overall clinical objectives
  • This individual must work independently, communicate and coordinate well with others on study and projects teams
  • IVD experience highly preferred, but not required