Department:

SOM KC Cancer Center Clinical Trials

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Clinical Research

Position Title:

Clinical Data Coordinator- Cancer Center

Job Family Group:

Professional Staff

Job Description Summary:

The Clinical Data Coordinator (CDC) will collect, abstract, review, document and monitor data related to clinical research projects. The CDC is responsible for working collaboratively with the Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator in the coordination and collection of data for cancer clinical trials. Additional responsibilities include involvement in the coordination of study start-up requirements and other duties that may be assigned by management staff.

The University of Kansas Cancer Center (KUCC) is the region's only National Cancer Institute designated comprehensive cancer center where patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.

This position may be eligible for a hybrid work schedule after 6 months based on management approval and department schedule. 

Job Description:

Required Qualifications

Education: Bachelors degree. A combination of education and relevant work experience may be substituted for degree on a year for year basis.

Work Experience:

• Basic proficiency in computer skills and clinical data entry.

• Previous knowledge of medical terminology.

• Strong communication as evidenced by application materials.

Preferred Qualifications

Certification: Research Certification

Work Experience:

• Previous oncology experience.

• Experience with database software.

• interpersonal and organizational skills.

• Detail oriented and ability to multi-task.

Job Duties Outlined:

• Responsible for overall knowledge of protocols as assigned.

• 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.

• Research and resolve data discrepancies; coordinate final database closure activities and participate in customer audits and process improvement initiatives.

• Perform other duties as assigned.

Required Documents:

• Resume/CV

• Cover letter

Comprehensive Benefits Package:

Employee Type:

Regular

Time Type:

Full time

Rate Type:

Hourly

Compensation Statement:

The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. 

Pay Range:

$26.13 - $39.20

Minimum

$26.13

Midpoint

$32.67

Maximum

$39.20