Responsibilities: Performing data verification of source documents; Conducting site visits, including pre-study, initiation, monitoring, and termination; Confirming adherence to all FDA, ICH-GCP, and local regulations; Ensuring implementation and compliance with FDA, and ICH-GCP guidelines. Qualifications: A minimum of 3 years of oncology experience as a CRA, Clinical Research Coordinator, and/or Research Nurse; Minimum of 1 year monitoring experience on an early phase trial.