Cancer Trials Data Coordinator

The University of Kansas Health System; Kansas City (MO); On-site; USD 39,000 - 53,000; Full time

Benefits offered by this job

Comprehensive benefits package

Day-one health coverage

Job summary

The University of Kansas Health System is seeking a Clinical Data Coordinator for the Cancer Center to collect, abstract, review and monitor data for cancer clinical trials. You will collaborate with Research Nurse Clinician and other staff to coordinate study start-up requirements and data collection.

This role requires strong attention to detail, experience in data entry, and familiarity with ICH/CFR/GCP guidelines.

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.
• Oncology experience preferred.
• Experience with database software preferred.
• Certifications/Licenses: CCRC/CCRP eligibility; CITI training encouraged.

Responsibilities

• Responsible for overall knowledge of protocols as assigned by the Director, Clinical Trials Office.
• Maintain screening/enrollment logs for each assigned protocol.
• Work collaboratively with the physician, nurse clinician, pharmacy and laboratory personnel to ensure tests/procedures/specimen collection per protocol.
• Communicate regarding patient data, status and protocol requirements with research staff.
• Conduct clinical trial data completion and query resolution for assigned protocols.
• Assist with identification and reporting of Adverse and Serious Adverse events per ICH/CFR/GCP and protocol.
• Attend study-specific trainings including Study Initiation and Internal Kick-off Meeting.
• Prepare and provide patient status reports as requested by the Director, Clinical Trials Office.
• Research and resolve data discrepancies; coordinate final database closure activities and participate in audits and process improvements.

Skills

Computer skills

Communication

Interpersonal

Organization

Attention to detail

Multi-tasking

Job description

The University of Kansas Health System is seeking a Clinical Data Coordinator for the Cancer Center to collect, abstract, review and monitor data for cancer clinical trials. You will collaborate with Research Nurse Clinician and other staff to coordinate study start-up requirements and data collection.

This role requires strong attention to detail, experience in data entry, and familiarity with ICH/CFR/GCP guidelines.