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
Assistant Clinical Investigator, Human Nutrition
By Office of Intramural Training & Education At , Bethesda, Md

National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, Maryland

Sub Investigator- Clinical Research
By Medix™ At Seattle, WA, United States
Provides medical management of adverse events as appropriate
Delegates study responsibilities as appropriate to trained study staff
Completes all study documentation in accordance with the study specific requirements
Prior experience in Clinical Research, preferably as a Sub Investigator
Ensures informed consent has been obtained prior to performing any study procedures
Documents all findings in subject specific source documents