As a Clinical Research Registered Nurse, I am responsible for the accurate completion of visit procedures and collection of information from study patients according to protocols, and for protecting the health, safety, and welfare of research participants. As a study coordinator, under the guidance and supervision of the Principal Investigator (PI) I have to ensure that assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines.