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.