- Basic proficiency in computer skills and clinical data entry.
- Previous knowledge of medical terminology.
- Strong communication as evidenced by application materials.
- Previous oncology experience.
- Experience with database software.
- interpersonal and organizational skills.
- Detail oriented and ability to multi-task.
- 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.
- Resume/CV
- Cover letter
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Clinical Data Coordinator- Cancer Center - Kansas City, United States - University of Kansas Medical Center
Description
Department:SOM KC Cancer Center Clinical Trials
Clinical ResearchPosition Title:
Clinical Data Coordinator- Cancer CenterJob Family Group:
Professional StaffJob 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.
The University of Kansas Medical Center and The University of Kansas Cancer Center are committed to creating and maintaining a diverse and inclusive learning and working environment, one that nurtures growth and development for all. We encourage individuals with diverse backgrounds to applyJob 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:
Certification: Research Certification
Work Experience:
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.
Employee Type:
RegularTime Type:
Full timeRate 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:
$ $39.20
Minimum
$26.13
Midpoint
$32.67
Maximum
$39.20
Clinical Data Coordinator- Cancer Center professionals in Kansas City
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Robert Sheehy
Healthcare Professional