Hello Upwok Family,
We are seeking an experienced Clinical Research Associate (CRA) or Clinical Trial Monitor to help prepare a candidate for the ICON CRA Monitoring Assessment.
The assessment consists of 6 sections and covers CRA monitoring concepts, clinical research best practices, site monitoring, GCP compliance, documentation review, and related topics.
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We are looking for someone who:
-Has hands-on CRA monitoring experience
-Has worked in pharmaceutical, biotech, CRO, or clinical trial environments
-Is familiar with ICON, IQVIA, Syneos, Parexel, Medpace, or similar CRO standards
-Can provide tutoring, coaching, practice questions, and test-preparation guidance
-Can identify knowledge gaps and help improve performance before the assessment
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Deliverables:
-Review assessment topics
-Conduct 1–3 tutoring sessions via Zoom
-Provide study recommendations and practice scenarios
-Help candidate understand monitoring concepts and industry expectations
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Preferred Qualifications:
-Former or current CRA
-Clinical Research Coordinator experience
-Clinical Trial Monitor experience
-GCP certification preferred
-Experience mentoring junior CRAs a plus
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If interested and available, please submit:
1. Your CRA experience
2. Your hourly rate
3. Whether you have helped candidates prepare for CRA assessments before
We look forward to workring with you.