Onsite
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Clinical Trials Data ManagementThis position will be based at our North Community Site.
Job Duties Outlined
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.
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.
Work Environment
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.
Required Qualifications
Work Experience:
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.
Preferred Qualifications
Certification: Research certification such as:
Certified Clinical Research Coordinator (CCRC) or certification eligible
Certified Clinical Research Professional (CCRP) or certification eligible
Collaborative Institutional Training Initiative (CITI) training certification
Work Experience:
Oncology experience.
Experience with database software.
Skills
Computer skills.
Communication.
Interpersonal.
Organization.
Attention to detail.
Multi-tasking.
Required Documents
Resume/CV
Cover Letter
Comprehensive Benefits Package:
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
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.
Minimum
$28.20Midpoint
$33.17Maximum
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