The main responsibilities include consenting patients prior to surgery, providing the tissue bank proper notification and documentation of consent, and managing regulatory components of the neuro logic tissue banking protocols and clinical data collection and management currently open at these hospitals.
Responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required.
The Clinical Research Coordinator is responsible for managing and assisting the Principal Investigator(s) and research team in the coordination of all activities of the study as required for successful implementation of the study protocol(s).
In this role, the selected candidate will participate in investigational drug studies through assisting in the design of dispensing protocols, maintaining drug records and inventory control, formulating dosages, monitoring patients and ensuring compliance with FDA and DEA regulations.