Clinical Data Coordinator I

Role: Clinical Data Coordinator supporting oncology clinical research within Caris's Precision Oncology Alliance. Responsibilities: abstracting and entering clinical data into electronic data capture (EDC) systems, ensuring data accuracy and quality, performing data verification and queries resolution, maintaining documentation, conducting QC audits, and supporting compliance with GCP, FDA, IRB, and HIPAA regulations. Also involves site visit coordination, source document management, and communication with research teams and investigators. Requirements: 3-5 years of experience in clinical data collection in GCP/regulatory settings, oncology-specific study experience, proficiency with EDC systems and Microsoft Office, strong medical terminology knowledge, and understanding of CDISC standards. Preferred: experience in both small and large-scale project management, mentoring, and training skills. High-value: oncology research, clinical data management, GCP compliance, FDA and IRB regulations, EDC proficiency. Collaboration with onsite teams, research staff, sponsors, and IRB; travel may be required. Work setup: unspecified, likely office-based with potential site visits.