Clinical Data Coordinator - Cancer Center
About The Position
The Clinical Data Coordinator (CDC) collects, abstracts, reviews, documents, and monitors data related to clinical research projects. The role works collaboratively with the Research Nurse Clinician, Clinical Research Coordinator, and Clinical Lab Coordinator to coordinate and collect data for cancer clinical trials. It also involves coordinating study start-up requirements and performing other duties assigned by management staff. The CDC maintains knowledge of assigned protocols and supports the conduct of clinical trials in accordance with ICH/CFR/GCP requirements. The position is in the University of Kansas Cancer Center Clinical Trials Data Management department.
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.
- Organization skills.
- Attention to detail.
- Ability to multitask.
Nice To Haves
- Oncology experience.
- Experience with database software.
- Certified Clinical Research Coordinator (CCRC) certification or eligibility for certification.
- Certified Clinical Research Professional (CCRP) certification or eligibility for certification.
- Collaborative Institutional Training Initiative (CITI) training certification.
Responsibilities
- Maintain overall knowledge of protocols as assigned by the Director, Clinical Trials Office.
- 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 with research staff about patient data, status, and protocol requirements.
- Conduct clinical trials in accordance with ICH/CFR/GCP and complete data requirements, including resolving queries for assigned protocols.
- Assist with identifying and reporting adverse and serious adverse events according to ICH/CFR/GCP and specific 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.
- Coordinate and collect data for cancer clinical trials and assist with 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.
- Long-term disability insurance.
- Additional voluntary insurance plans.
- Paid vacation and sick leave 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).
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What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
