Cancer Trials Clinical Data Coordinator

Kumc; Texas; On-site; USD 39,000 - 53,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Long-term disability insurance

Employer-paid life insurance

Paid time off

Job summary

The University of Kansas Medical Center is seeking a Clinical Data Coordinator for the Cancer Center to collect, abstract, review, and monitor data across cancer clinical trials. You will collaborate with trial staff to ensure data integrity, assist with study start-up requirements, and support data quality initiatives.

Experience in clinical data entry and medical terminology is required, with oncology exposure preferred.

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

• 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, etc. are obtained per protocol.
• Communicate regarding patient data, status and protocol requirements with research staff.
• Conduct clinical trial in accordance with ICH/CFR/GCP and responsible for all data completion; query resolution for assigned protocols.
• Assist with the identification and reporting of Adverse and Serious Adverse events in accordance with ICH/CFR/GCP and specific protocol.
• Attend study specific training to include but not limited to Study Initiation and Internal Kick-off Meeting.
• Prepare and provide patient status report as requested by the Director, Clinical Trials Office.
• Research and resolve data discrepancies; coordinate final database closure activities and participate in customer audits and process improvement initiatives.

Skills

Computer skills

Communication

Interpersonal

Organization

Attention to detail

Multi-tasking

Job description

The University of Kansas Medical Center is seeking a Clinical Data Coordinator for the Cancer Center to collect, abstract, review, and monitor data across cancer clinical trials. You will collaborate with trial staff to ensure data integrity, assist with study start-up requirements, and support data quality initiatives.

Experience in clinical data entry and medical terminology is required, with oncology exposure preferred.