Clinical Data Coordinator - Cancer Trials & Research

University of Kansas Medical Center; Kansas City (KS); On-site; USD 39,000 - 53,000; Full time

Benefits offered by this job

Health, dental, vision insurance

Paid time off & holidays

Retirement plan

Job summary

The University of Kansas Cancer Center is seeking a Clinical Data Coordinator to collect, abstract, review, document and monitor data for cancer clinical trials. Collaborate with Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator to coordinate data collection and start-up requirements.

Responsibilities include log maintenance, data entry, protocol adherence, adverse event reporting, and data queries.

Qualifications

• 4 years of relevant work experience. Education may substitute for experience on a year for year basis.
• Experience with clinical data entry and medical terminology.

Responsibilities

• Maintain protocols knowledge as assigned by the Director, Clinical Trials Office.
• Maintain screening/enrollment logs for each protocol.
• Coordinate with physicians, nurses, pharmacy and lab to ensure tests/procedures/specimens meet protocol.
• Communicate patient data, status and protocol requirements with research staff.
• Ensure data completion and resolve queries per protocol; adhere to ICH/CFR/GCP.
• Identify and report Adverse events per ICH/CFR/GCP and protocol.
• Attend study trainings including Initiation and Kick-off meetings.
• Prepare patient status reports for the Director, Clinical Trials Office.
• Resolve data discrepancies and participate in audits and process improvements.

Skills

Computer skills

Communication

Interpersonal

Organization

Attention to detail

Multi-tasking

Tools

Database software

Job description

The University of Kansas Cancer Center is seeking a Clinical Data Coordinator to collect, abstract, review, document and monitor data for cancer clinical trials. Collaborate with Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator to coordinate data collection and start-up requirements.

Responsibilities include log maintenance, data entry, protocol adherence, adverse event reporting, and data queries.