DescriptionThe Clinical Research Supervisor oversees moderate/complex research study coordination. In this role you will manage unit operations to ensure compliance with departmental and organizational policies, procedures, and defined internal controls. Supervise operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. Oversee planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). Serve as liaison with the Principal Investigator (PI), ancillary