Job Summary

• We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within the South East.
• You will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and procedures, quality standards, and adverse event reporting requirements.
• We offer an opportunity to shape clinical research at high-performing sites and contribute to global development programs in a collaborative environment with growth, mentorship, and continuous improvement.

Matching Summary

Skills & Requirements

Key Requirements

• Bachelor’s degree or higher
• Extensive direct site management experience
• Fluent in English
• Valid driver’s license preferred

Work Rights