Not specified; not specified; competitive compensa...
Fully remote with travel (65-75%)
Ich/gcp compliance knowledge
Site management and monitoring
Protocol adherence expertise
The company is seeking a Clinical Research Associate (CRA) to oversee site management and compliance for clinical studies in North West England, with a significant travel requirement. The ideal candidate should have robust knowledge of clinical research regulations and experience in site management, with a strong emphasis on building relationships and mentoring junior staff
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 to ensure data integrity, subject safety, and protection of rights 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 mentorship.
Matching Summary
Match Score: 85
The company is seeking a Clinical Research Associate (CRA) to oversee site management and compliance for clinical studies in North West England, with a significant travel requirement. The ideal candidate should have robust knowledge of clinical research regulations and experience in site management, with a strong emphasis on building relationships and mentoring junior staff.
Salary
Not specified; Not specified; Competitive compensation and benefits