Clinical Research Sub Investigator - 211452
By Medix™ At Fayetteville, NC, United States
Provides medical management of adverse events as appropriate
Performs all job responsibilities in accordance with standards of Good Clinical Practice
Delegates study responsibilities as appropriate to trained study staff
Possesses a working knowledge of GCP/ICH guidelines, Clinic SOPs, QA/QC procedures, and Investigator 1572 Form
Performs all study responsibilities in compliance with the IRB approved protocol
Completes all study documentation in accordance with the study specific requirements