Celline Mitchell

Study Coordinator @Orita Clinical Research, Llc

Decatur, GA, US

Manage the daily operations of clinical trials, to include; following the protocol according to the Schedule of activities for each visit, IP accountability, and data management Ensure all data for the clinical trial has been entered correctly on source documents and into assigned EDC for the clinical trial. Respond to queries in a timely manner. Maintain accurate filing and documentation in the regulatory binder. Adhere to Good Clinical Practice, ICH, IRB, FDA, and other regulatory guidelines and requirements as a priority to protecting patient rights and safety and the integrity of the clinical study.

Savannah State University

Bachelor's degree