Fully remote with travel (approximately 65–75% of working time)
Ich/gcp compliance knowledge
Site management and monitoring
Protocol adherence expertise
The job posting is for a Clinical Research Associate (CRA) position in North West England with a focus on managing clinical research sites and ensuring compliance with regulatory standards. The role requires significant travel and emphasizes strong communication, leadership, and clinical research knowledge
Job Summary
The role involves leading performance and compliance for assigned protocols and sites while ensuring rigorous adherence to ICH/GCP standards.
Candidates will perform remote and on-site monitoring activities to ensure data integrity, subject safety, and regulatory compliance across all trial phases.
The position offers the opportunity to shape clinical research at high-performing sites within a collaborative environment focused on growth and continuous improvement.
Matching Summary
Match Score: 85
The job posting is for a Clinical Research Associate (CRA) position in North West England with a focus on managing clinical research sites and ensuring compliance with regulatory standards. The role requires significant travel and emphasizes strong communication, leadership, and clinical research knowledge.