Clinical Research Associate

Job Summary

To support a leading clinical research organization advancing innovative oncology studies, the remote Clinical Research Associate (CRA) will ensure study sites operate efficiently, maintain regulatory compliance, and execute clinical trial protocols while collaborating with investigators and site personnel.

Key responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits while ensuring compliance with GCP and ICH guidelines
• Partner with study sites to develop and implement recruitment plans to meet enrollment and project goals
• Track regulatory submissions, patient recruitment, and study progress to ensure milestones are achieved

Required qualifications

• Bachelor's degree in a scientific discipline, healthcare, or a related field preferred
• Minimum of three (3) years of on-site monitoring experience in oncology clinical trials
• Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Experience supporting oncology protocols and clinical research studies
• Proficiency with Microsoft Office applications