Oncology Clinical Research Associate

Job Summary

To support a global clinical program, the fully remote Oncology Clinical Research Associate will conduct site visits, ensure compliance with regulatory standards, and collaborate with investigative sites to optimize patient recruitment and study execution while traveling within the U.S.

Key responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits to ensure compliance with GCP, ICH, and protocol requirements
• Partner with investigative sites to develop and execute patient recruitment and enrollment strategies to meet study objectives
• Monitor study conduct, assess protocol adherence, and maintain essential trial documentation to support regulatory compliance and data integrity

Required qualifications

• Bachelor's degree in a scientific, life sciences, healthcare, or related discipline preferred
• Minimum of 3 years of recent on-site clinical monitoring experience in Oncology, specifically supporting Phase I studies
• Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and oncology clinical trial protocols
• Proven ability to independently manage investigative sites and ensure high standards of data quality and patient safety
• Proficiency with Microsoft Office applications and demonstrated ability to manage timelines and budgets effectively