The Clinical Research Supervisor oversees moderate/complex research study coordination.  They will supervise unit operations to ensure compliance with departmental and organizational policies, procedures, and defined internal controls.  They will also supervise operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. They oversee the 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). They will serve as liaison with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. The responsibilities outlined in the job description provide a general overview of duties and tasks performed the role. Performance of duties and tasks will vary based on the department operations, the type of study and scope of service.

Salary Range: $92,600.00 – 202,200.00 Annually