Sr. CRA/Clinical Research Associate, Oncology - St. Louis - (St Louis, MO)

Sr. CRA role will be focused mostly on monitoring sites in the Midwest: · Expedites the pre-study and study initiation processes including the conduct of Pre-Study valuation and Site Initiation visits. · Conducts Site Initiation visits in collaboration with Site Managers and/or Protocol Managers, to orient and train site personnel regarding the protocol and applicable regulatory requirements. · Identifies, evaluates, and recommends potential investigators/sites on an on-going to assist in the placement of planned clinical studies with qualified investigators. · Critically reviews and analyzes site activities through frequent visits and contacts to monitor study sites following the monitoring plan and applicable SOPs, to assure compliance with the protocol, ICH and/or FDA GCP Guidelines and other local regulations. This includes, but is not limited to: - Manages multiple protocols, across therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory.