Clinical Research Coordinator - Nuclear Medicine and Theranostics

Benefits

Responsibilities

• •The Department of Nuclear Medicine and Theranostics is seeking a detailed and dynamic Clinical Research Coordinator
• •In this role, you will coordinate research studies, identify participants, and assist the Principal Investigator (PI) with patient eligibility
• •Responsibilities also include facilitating the informed consent process, educating participants about protocol requirements, and emphasizing the significance of protocol compliance
• •The role requires maintaining all necessary documentation in accordance with FDA regulations, Good Clinical Practice (GCP) guidelines, and the funding source
• •This includes managing patient registration, data, and treatment assignment
• •This role will involve quality control and assurance activities related to study workflows and documentation
• •In addition, the Clinical Research Coordinator is responsible for procuring and distributing study supplies, including coordinating specimen collection and shipping
• •Ensuring the safe and accurate completion of protocol-required procedures according to regulatory guidelines, FDA CFR, GCP, and institutional best practices is essential
• •5 more items(s)