Want to know if this job is worth applying to?
Kansas City Metro Area, United States of America
Onsite
-----
CCRJob Responsibilities
Responsible for overall knowledge of protocols as assigned.
Create and maintain logs, data base or data registry.
Work collaboratively with the physician, nurse clinicians, pharmacy, and laboratory personnel to ensure data is obtained per protocol and correct.
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 required by position, to include but not limited to Study Initiation.
Prepare and provide patient status report.
Research and resolve data discrepancies; coordinate any database 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.
Required Qualifications
Work Experience: Four years of experience with clinical data entry, medical/clinical research and medical terminology. Relevant education may be substituted on a year-for-year basis.
Preferred Qualifications
Education: Bachelor's degree in applicable field of study.
Certifications: Research certification such as: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or Association of Clinical Research Professionals (ACRP).
Work Experience:
Experience in department field of research, reviewing patient data/medical records or working with research participants.
Experience with database software, SPSS statistical software and REDCap.
Skills
Computer skills.
Communication.
Interpersonal skills.
Organization skills.
Attention to detail.
Multi-tasking.
Required Documents
Resume
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
$38.35