Develop presentation material and present during face-to-face Sponsor meetings (i.e., Kick-off Meetings, Investigator Meetings)
Coordinate final medical review of study report narratives and submission to Medical Writers
Develop drafts of adjudication material (i.e., charter, reporting materials)
Provide periodic safety summaries to project Data Manager, Clinical Trial Manager, and Medical Monitor
Train new Clinical Safety Coordinators on safety reporting responsibilities
Coordinate safety responsibilities for aggregate reporting purposes (e.g., ensure timely data entry, tracking of pending cases, collaborate with Medical Monitor and Regulatory Affairs)
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