Oncology CRA II

Responsibilities: of the Oncology CRA II: • Conduct site qualification, initiation, routine monitoring, and closeout visits for oncology clinical trials. • Ensure compliance with ICH-GCP guidelines, study protocols, sponsor requirements, and applicable regulatory standards. • Review source documentation and verify clinical trial data for accuracy, completeness, and consistency. • Identify, document, and resolve site issues, protocol deviations, and data discrepancies. • Develop strong relationships with investigators, study coordinators, and site personnel. • Support patient recruitment, retention efforts, and study enrollment goals. • Prepare monitoring reports and maintain trial master file documentation. • Collaborate with cross-functional clinical operations teams to ensure successful study execution. Requirements of the Oncology CRA II: • Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field. • 3+ years of clinical monitoring experience as a CRA with oncology trial experience. • Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes. • Experience conducting site monitoring visits independently. • Proficiency with EDC systems, CTMS platforms, and clinical trial documentation. Compensation: for the Oncology CRA II: • Salary range: $115,000 - $127,000 base salary • Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.