As the primary study contact at the CRO for sites conducting clinical research studies:- Monitors patient safety within clinical trials- Ensures sites follow the sponsors protocol- Reports and follows site findings to completions- Ensures thats essential documents are collected, tracked, filed, and meet ALCOA standards- Reviews EDC and issues queries for data that needs clarification or is inconsistent - Completes scheduled and ad-hoc site managment contacts to support sites with their study responsibilities