Sr Clinical Research Associate (2221) - (San Mateo, CA)

Overview: Manage wide variety of activities to support the clinical research programs to ensure studies are completed on time, within budget, and in compliance with Good Clinical Practice (GCP), government regulations, and overall clinical objectives. Responsibilities: Daily activities will vary depending on the clinical phase of the program. Will have responsibilities for managing multiple projects within a program or may manage a single project. Determine methods and procedures for performing new assignments. Provide mentorship to clinical vendor CTAs and CRAs. Responsible for as aspects of clinical program including but not limited to: training, oversight of clinical vendor monitors and study site staff personnel, and development of standardized clinical oversight/tracking tools. Responsible for quality study oversight, including but not limited to monitoring, oversee clinical site staff, in addition to clinical vendors and clinical vendor Monitors, and review monitoring trip reports.