Also referred to as:
VP of Clinical Data Monitoring, VP of Clinical Research Onsite Monitoring
Requirements and Responsibilities
VP of Clinical Research Monitoring plans and leads all clinical research monitoring activities within an organization. Implements and executes strategic plans and goals. Being a VP of Clinical Research Monitoring provides leadership and oversight to the design and development of processes. Designs policies and procedures to ensure all clinical research trials adhere to established processes and procedures, FDA regulatory requirements, Good Clinical Practice (GCP) research standards, and all other applicable regulatory requirements. Additionally, VP of Clinical Research Monitoring may require an advanced degree. May require ACRP or SOCRA certification. Typically reports to senior management. The VP of Clinical Research Monitoring manages a departmental function within a broader corporate function. Develops major goals to support broad functional objectives. Approves policies developed within various sub-functions and departments. To be a VP of Clinical Research Monitoring typically requires 8+ years of managerial experience. Comprehensive knowledge of the overall departmental function.
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