Oncology Clinical Data Coordinator

Kumc; Kansas City (MO); On-site; USD 39,000 - 53,000; Full time

Benefits offered by this job

Health, dental, vision insurance

Paid time off and holidays

Retirement plan with employer contrib.

Job summary

University of Kansas Medical Center’s Cancer Center seeks a Clinical Data Coordinator to manage data for cancer clinical trials. You will collect, abstract and review data, working with trial team members to ensure protocol compliance and timely data completion.

Preferred candidates have oncology exposure and experience with database software, ICH/GCP guidelines, and adverse event reporting. This hourly role supports startup activities and data audits within a comprehensive cancer center.

Qualifications

• 4 years of relevant work experience (education may substitute for experience).
• Experience with clinical data entry and medical terminology.
• Oncology experience preferred.
• Experience with database software.

Responsibilities

• Collect, abstract, review, document and monitor data for cancer clinical trials.
• Work with the Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator to coordinate data collection per protocol.
• Assist with study start-up requirements and related duties as assigned.
• Ensure data completion and perform query resolution for assigned protocols.
• Support adverse event reporting in line with ICH/GCP guidelines.
• Prepare patient status reports and participate in audits and process improvements.

Skills

Communication

Interpersonal

Organization

Attention to detail

Multi-tasking

Education

Bachelor's degree or equivalent experience

Tools

Database software

Job description

University of Kansas Medical Center’s Cancer Center seeks a Clinical Data Coordinator to manage data for cancer clinical trials. You will collect, abstract and review data, working with trial team members to ensure protocol compliance and timely data completion.

Preferred candidates have oncology exposure and experience with database software, ICH/GCP guidelines, and adverse event reporting. This hourly role supports startup activities and data audits within a comprehensive cancer center.