Senior Clinical Research Associate

Job Summary

A company is looking for a Senior Clinical Research Associate (CRA).

Key Responsibilities

• Monitor clinical trial sites for adherence to protocols, regulatory requirements, and GCP standards
• Conduct site visits to assess performance, resolve issues, and support trial execution
• Collaborate with cross-functional teams for timely and accurate data collection and reporting

Required Qualifications and Education

• Advanced degree in life sciences, nursing, or medicine
• Extensive experience as a Clinical Research Associate with knowledge of clinical trial processes
• Minimum of 12 months of independent monitoring experience
• Proven ability to manage multiple sites and projects simultaneously
• Expertise in monitoring practices and proficiency in clinical trial software