Clinical Data Coordinator - Cancer Center

University of Kansas Medical Center • Kansas City, KS

1d

About The Position

The Clinical Data Coordinator (CDC) collects, abstracts, reviews, documents, and monitors data for clinical research projects, particularly cancer clinical trials. The role works collaboratively with the Research Nurse Clinician, Clinical Research Coordinator, and Clinical Lab Coordinator to coordinate and collect trial data. Additional duties include helping coordinate study start-up requirements and other tasks assigned by management. The coordinator is responsible for overall knowledge of assigned protocols and for completing and resolving queries for assigned trials in accordance with applicable standards. Duties and responsibilities may change, and this description is not exhaustive.

Requirements

• Four years of relevant work experience; education may substitute for experience on a year-for-year basis.
• Experience with clinical data entry and medical terminology.
• Computer skills.
• Communication skills.
• Interpersonal skills.
• Organizational skills.
• Attention to detail.
• Ability to multitask.

Nice To Haves

• Oncology experience.
• Experience with database software.
• Certified Clinical Research Coordinator (CCRC) certification or eligibility.
• Certified Clinical Research Professional (CCRP) certification or eligibility.
• Collaborative Institutional Training Initiative (CITI) training certification.

Responsibilities

• Maintain screening and enrollment logs for each assigned protocol.
• Work with physicians, nurse clinicians, pharmacy, and laboratory personnel to ensure tests, procedures, and specimen collection are completed according to protocol.
• Communicate patient data, status, and protocol requirements with research staff.
• Conduct clinical trials in accordance with ICH/CFR/GCP and complete all required data; resolve queries for assigned protocols.
• Assist with identifying and reporting adverse and serious adverse events in accordance with ICH/CFR/GCP and study protocols.
• Attend study-specific training, including Study Initiation and Internal Kick-off Meetings.
• 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.
• Assist with coordination of study start-up requirements.

Benefits

• Health, dental, and vision insurance coverage beginning on day one.
• Health expense accounts with employer contributions for employees participating in a qualifying health plan.
• Employer-paid life insurance and long-term disability insurance.
• Additional voluntary insurance plans.
• Paid vacation and sick time accruing upon hire.
• Ten paid holidays.
• One paid discretionary day after six months of employment.
• Paid bereavement, jury duty, military service, and parental leave after 12 months of employment.
• Retirement program with an employer contribution.
• Additional voluntary retirement programs (457 or 403b).

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed