Clinical Research Associate

Job Summary

To ensure the integrity of clinical trials, the full-time remote Clinical Research Associate will monitor study progress, verify data accuracy, and support site compliance and training throughout all phases of clinical studies.

Key responsibilities

• Conduct source verification and resolve data discrepancies while ensuring informed consent accuracy
• Communicate effectively with clinical sites and project teams through monitoring reports and correspondence
• Ensure site personnel are trained and compliant with study protocols and applicable regulations

Required qualifications

• University degree or equivalent combination of education and experience
• 1-3 years of relevant experience in clinical research