Salary: $35/HR-$38/HR (Based on experience, education, certifications). Benefits offered by employer.
Requirements:
Day to Day: You'll be responsible for ensuring the collection of data and patient information is accurate and consistent, while working in compliance with FDA regulations, Good Clinical Practices (GCP), and study-specific protocols. You will also interact directly with patients, guiding them through the research process, answering questions, and ensuring their well-being and informed consent.
Overview: As a Oncology Clinical Research Coordinator , you will conduct professional research and provide study services across both inpatient and outpatient settings. Your responsibilities will include 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 you 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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