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. -------------------------------------------------- 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 -------------------------------------------------- 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 -------------------------------------------------- Preferred Qualifications -Former or current CRA -Clinical Research Coordinator experience -Clinical Trial Monitor experience -GCP certification preferred -Experience mentoring junior CRAs a plus -------------------------------------------------- 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. Apply To this Job