Clinical Data Coordinator
About The Position
The Clinical Data Coordinator will collect, abstract, review, document and monitor data related to clinical research projects. The Clinical Data Coordinator 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.
Requirements
- 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.
- Computer skills.
- Communication.
- Interpersonal skills.
- Organization.
- Attention to detail.
- Multi-tasking.
- Resume
- Cover Letter
Nice To Haves
- Research certification such as:
- Certified Clinical Research Coordinator (CCRC).
- Certified Clinical Research Professional (CCRP).
- Collaborative Institutional Training Initiative (CITI) training certification.
- Oncology experience.
- Experience with database software.
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.
Benefits
- Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan.
- Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available.
- Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays.
- One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment.
- A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available.
- https://www.kumc.edu/human-resources/benefits.html
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Hospitals
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
