Summarized Purpose:
Study coordinator to support ongoing large clinical study in US. Completes all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interacts with the research site team and other interdepartmental staff. Engages in the entire site operations process, which includes recruitment, enrollment, retention of study participants, data entry and query resolution.

Essential Functions:
" Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
" Provides medical care to patients, always ensuring patient safety comes first.
" Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized.
" Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests...