Description

The Clinical Research Center Supervisor provides immediate
supervision to routine research study coordination. This position supervises
unit operations to ensure compliance with departmental and organizational
policies, procedures, and defined internal controls. Supervises operational
management of clinical research/trial/study activities from design, set up,
conduct, through closeout. The Supervisor oversees 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). Serves 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...