Qureos Mentor

Intellectt Inc

<div>
 
 
 Job Title: Clinical Research Associate (CRA)
 
 
 
 
 Location:
 
 
 Lake Forest, IL (Onsite)
 
 
 
 
 Duration:
 
 
 12 Months
 
 
 
 
 
 
 Job Summary:
 
 
 
 We are seeking an experienced
 
 Clinical Research Associate (CRA)
 
 to support IVD and specimen collection studies. The role involves site monitoring, study coordination, and regulatory support while ensuring compliance with
 
 ICH GCP, FDA, and IRB guidelines
 
 .
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Support study planning, execution, and coordination
 </li>
 <li>
 Perform site selection, initiation, monitoring, and close-out activities
 </li>
 <li>
 Manage investigator sites and act as primary point of contact
 </li>
 <li>
 Ensure protocol adherence and timely patient enrollment
 </li>
 <li>
 Prepare and review regulatory documents, study protocols, and reports
 </li>
 <li>
 Review medical records and source documentation
 </li>
 <li>
 Manage CRF collection, data review, and cleanup
 </li>
 <li>
 Participate in study meetings and contribute to study summaries
 </li>
 <li>
 Mentor junior CRAs and support lead CRA activities
 </li>
 </ul>
 
 
 Required Skills &amp; Experience:
 
 
 <ul>
 <li>
 5+ years of clinical research monitoring experience
 </li>
 <li>
 Strong knowledge of
 
 ICH GCP, FDA, and IRB regulations
 
 </li>
 <li>
 Hands-on experience in site monitoring and management
 </li>
 <li>
 Experience with source data verification and medical record review
 </li>
 <li>
 Strong communication and stakeholder management skills
 </li>
 <li>
 Leadership or mentoring experience
 </li>
 </ul>
</div>

Clinical Research Associate (CRA)

Join Intellectt Inc and explore 1   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Intellectt Inc

About Company

Clinical Research Associate (CRA)