Clinical Data Monitor

Job Summary

To support critical oncology research efforts, the full-time Clinical Data Monitor will manage clinical data activities remotely, ensuring data integrity and quality while overseeing investigative sites and collaborating with research coordinators on patient enrollment and data collection.

Key responsibilities

• Perform quality control reviews of Case Report Forms (CRFs) and source documents, issuing data queries as needed
• Maintain regulatory documentation for assigned sites and provide training and feedback to Clinical Research Coordinators
• Ensure compliance with GCP guidelines and other regulatory standards while collaborating with research teams and stakeholders

Required qualifications

• 3-5 years of experience in data collection within a GCP regulated clinical research environment
• Proficiency in Microsoft Office Suite and experience with Electronic Data Capture (EDC) systems
• Clinical study experience in oncology and strong understanding of medical terminology
• Ability to work independently, prioritize tasks, and manage multiple projects effectively
• Bachelor's degree preferred, along with Research Coordinator certification (SoCRA, ACRP) as a plus