Clinical Data Monitor I

Role: Clinical Data Monitor overseeing data management for oncology-focused clinical research at Caris. Objectives: ensure data integrity and quality supporting cancer treatment research. Responsibilities: manage clinical data collection, perform source data verification, generate data queries, maintain regulatory documentation, and conduct quality control audits in compliance with GCP, FDA, IRB, HIPAA, and SOPs. Support site staff training on EDC systems, foster strong site relationships, and collaborate with research teams. Requirements: 3-5 years of GCP-regulated clinical research experience, proficiency in EDC and Microsoft Office, with oncology-specific clinical study background. Preferred: Bachelor’s degree, research certification (SoCRA/ACRP), knowledge of human anatomy. High-Value: Oncology (cancer), clinical data management, GCP compliance, EDC systems, study monitoring. Work setup: likely in an office setting, may involve working weekends or holidays, with standard safety and compliance training.