Clinical Data Coordinator

• Abstract clinical data from subject source documentation
• Enter clinical data into study-specific EDC case report forms
• Clean clinical data to verify accuracy
• Update EDC following verification of subject data and resolve data queries
• Track site goals and case report form completion
• Prioritize site cases for analysis
• Maintain study-specific documentation
• Perform quality-control audits of the clinical database
• Support and adhere to GCP, FDA, IRB, HIPAA, site operating procedures, and ethical standards
• Confirm appropriate consenting is performed and documented before data abstraction
• Maintain source document management and request information according to Caris and site requirements
• Act as site designated entry person
• Communicate with the research team, investigators, Clinical Research Associates, study sponsor, and ancillary staff
• Schedule on-site visits to perform data review and EDC data entry

Explore Clinical Data Coordinator I at Caris Life Sciences. Review requirements and application details.