Clinical Data Coordinator - Cancer Center

h2bDepartment:/b/h2SOM KC Cancer Center Clinical Trialsp style="text-align:inherit"-----/pClinical Trials Data Managementh2bPosition Title:/b/h2Clinical Data Coordinator - Cancer Centerh2bJob Family Group: /b/h2Professional Staffh2bJob Description Summary:/b/h2The 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.brbrThe 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.h2bJob Description:/b/h2pspan style="color:#000000"buspan style="font-size:14px"Job Duties Outlined/span/u/b/span/pullipspan style="color:#000000"span style="font-size:14px"Responsible for overall knowledge of protocols as assigned by the Director, Clinical Trials Office./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Maintain screening/enrollment logs for each assigned protocol./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Work collaboratively with the physician, nurse clinician, pharmacy and laboratory personnel to ensure tests/procedures/specimen collection, etc. are obtained per protocol./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Communicate regarding patient data, status and protocol requirements with research staff./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Conduct clinical trial in accordance with ICH/CFR/GCP and responsible for all data completion; query resolution for assigned protocols./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Assist with the identification and reporting of adverse and serious adverse events in accordance with ICH/CFR/GCP and specific protocol./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Attend study specific training to include but not limited to study initiation and internal kick-off meeting./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Prepare and provide patient status report as requested by the Director, Clinical Trials Office./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Research and resolve data discrepancies; coordinate final database closure activities and participate in customer audits and process improvement initiatives./span/span/p/li/ulp/ppspan style="color:#000000"span style="font-size:14px"This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. /span/span/pp/ppspan style="color:#000000"buspan style="font-size:14px"Work Environment: /span/u/bspan style="font-size:14px"This position may be eligible for a hybrid work schedule after 6 months. Incumbent will work remotely and on campus based on a set departmental schedule based on management approval and must reside in the greater Kansas City metropolitan area./span/span/pp/ppspan style="color:#000000"buspan style="font-size:14px"Required Qualifications/span/u/b/span/ppspan style="color:#000000"bspan style="font-size:14px"Work Experience/span/bspan style="font-size:14px":/span/span/pullipspan style="color:#000000"span style="font-size:14px"4 years of relevant work experience. Education may substitute for experience on a year for year basis./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Experience with clinical data entry and medical terminology./span/span/p/li/ulp/ppspan style="color:#000000"buspan style="font-size:14px"Preferred Qualifications/span/u/b/span/ppspan style="color:#000000"bspan style="font-size:14px"Certification:/span/bspan style="font-size:14px" Research certification such as: /span/span/pullipspan style="color:#000000"span style="font-size:14px"Certified Clinical Research Coordinator (CCRC)./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Certified Clinical Research Professional (CCRP)./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Collaborative Institutional Training Initiative (CITI) training certification./span/span/p/li/ulpspan style="color:#000000"bspan style="font-size:14px"Work Experience:/span/b/span/pullipspan style="color:#000000"span style="font-size:14px"Oncology experience./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Experience with database software./span/span/p/li/ulp/ppspan style="color:#000000"buspan style="font-size:14px"Skills/span/u/b/span/pullipspan style="color:#000000"span style="font-size:14px"Computer skills./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Communication./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Interpersonal skills./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Organization./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Attention to detail./span/span/p/lilipspan style="color:#000000"span style="font-size:14px"Multi-tasking./span/span/p/li/ulp/ppbComprehensive Benefits Package:/b/pdivdivdivdivpCoverage 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. spanspana href="https://www.kumc.edu/human-resources/benefits.html" target="_blank"https://www.kumc.edu/human-resources/benefits.html/a/span/span/pp/pp/p/div/div/div/divh2bEmployee Type: /b/h2Regularh2bTime Type: /b/h2Full timeh2bRate Type: /b/h2Hourlyp style="text-align:inherit"/pp style="text-align:left"bCompensation Statement:/b/pp style="text-align:left"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. /pp style="text-align:inherit"/ph2bPay Range:/b/h2$28.20 - $38.35p style="text-align:left"bMinimum/b/p$28.20p style="text-align:left"bMidpoint/b/p$33.17p style="text-align:left"bMaximum/b/p$38.35