Clinical Data Coordinator - Cancer Center

Clinical Data Coordinator - Cancer Center Department

SOM KC Cancer Center Clinical Trials – Clinical Trials Data Management

Clinical Data Coordinator - Cancer Center

Professional Staff

The Clinical Data Coordinator (CDC) will collect, abstract, review, document and monitor data related to clinical research projects. The CDC works collaboratively with the Research Nurse Clinician, Clinical Research Coordinator and Clinical Lab Coordinator to coordinate and collect 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.

• Maintain overall knowledge of protocols as assigned by the Director, Clinical Trials Office.
• Maintain screening/enrollment logs for each assigned protocol.
• Work with physician, nurse clinician, pharmacy and laboratory personnel to ensure tests/procedures/specimen collection 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 be responsible for all data completion; resolve queries for assigned protocols.
• Assist with identification and reporting of Adverse and Serious Adverse events per ICH/CFR/GCP and protocol.
• Attend study‑specific training, 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 customer audits and process improvement initiatives.

This position may be eligible for a hybrid work schedule after 6 months. The incumbent will work remotely and on campus according to a departmental schedule approved by management and must reside in the greater Kansas City metropolitan area.

• 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.

• Research certifications such as Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) or CITI training certification.
• Oncology experience.
• Experience with database software.

• Computer skills.
• Communication.
• Interpersonal.
• Organization.
• Attention to detail.
• Multi‑tasking.

Resume/CV, Cover Letter.

Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions.

Employer‑paid life insurance, long‑term disability insurance, and various voluntary insurance plans are available.

Paid time off, including vacation and sick leave, accrues upon hire, plus ten paid holidays. One paid discretionary day is available after 6 months, and additional PTO for bereavement, jury duty, military service, and parental leave is available after 12 months.

A retirement program with generous employer contributions and additional voluntary programs (457 or 403b) are available. For more information, visit https://(Use the "Apply for this Job" box below)..html

Regular

Full time

Hourly

The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. Factors considered include education, experience, training, qualifications relative to the requirements of the position, and funding. At KU 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.

• Minimum: $26.13
• Midpoint: $32.67
• Maximum: $39.20

To learn more and apply online, visit  or go to  and search for position number JR009442.

Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or other website will NOT be reviewed or…