Screening, enrolling, and monitoring clinical research patients/volunteers, ensuring that all activities are carried out according to FDA guidelines and study protocols. This role requires the candidate to closely monitor patient progress, provide timely and accurate reporting, and ensure adherence to safety standards throughout the clinical trial process
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3 Years of clinical trials experience in a hospital - outpatient experience
Oncology experience
Experience being patient facing
BLS (Basic Life Support)
Certified CRC (Clinical Research Coordinator)
Good Practice Cert
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.