Oncology Clinical Research Associate

To support a global clinical program, the fully remote Oncology Clinical Research Associate will conduct site visits, ensure compliance with regulatory standards, and partner with investigative sites to enhance patient recruitment and enrollment strategies.Key responsibilities:Conduct site selection, initiation, monitoring, and close-out visits to ensure compliance with GCP, ICH, and protocol requirementsPartner with investigative sites to develop and execute patient recruitment and enrollment strategies to meet study objectivesMonitor study conduct, assess protocol adherence, and maintain essential trial documentation to support regulatory compliance and data integrityRequired qualifications:Bachelor's degree in a scientific, life sciences, healthcare, or related discipline preferredMinimum of 3 years of recent on-site clinical monitoring experience in Oncology, specifically with Phase I studiesStrong knowledge of Good Clinical Practice (GCP), ICH guidelines, and oncology clinical trial protocolsProven ability to independently manage investigative sites and ensure high standards of data quality and patient safetyProficiency with Microsoft Office applications and demonstrated ability to manage timelines and budgets effectively