$75,000–$124,000
USD/year
Perform centralized and prompt monitoring activities for Phase I-IV clinical research and/or non-interventional studies (NIS) in accordance with project plans, the protocol, ICH-GCP, and all applicable local and federal regulatory requirements while ensuring patient safety and data integrity using a variety of statistical and analytical tools. Analyze site and study level data in the applicable data analytics tool(s) and may identify risks and trends at the site and study level, as well as operational performance issues.