À propos de ce poste Clinical Research Coordinator - Internal Medicine (Diabetes Institute) chez University of Kansas Medical Center
Department:
SOM KC The Diabetes Institute (DI)-----
Diabetes InstitutePosition Title:
Clinical Research Coordinator - Internal Medicine (Diabetes Institute)Job Family Group:
Professional StaffJob Description Summary:
The Clinical Research Coordinator in the KU Diabetes Institute works collaboratively with multidisciplinary teams, research staff, and participants to support the coordination of clinical research studies related to diabetes, weight management, physical activity, and nutrition. Responsibilities include recruiting, screening, and educating participants; managing study activities such as data collection, documentation, and analysis; monitoring participant progress and adverse events; and participating in quality assurance audits to ensure compliance with study protocols and regulatory standards.Job Description:
Job Duties
Study Support & Logistics:
- Assist in recruitment, evaluation, and education of participants regarding clinical trials following established procedures and protocols.
- Ensure adequate study supplies are maintained and assist with tracking study visits, expenditures, and reimbursement requests for study-related items.
- Maintain trial regulatory documentation files as directed, including correspondence with sponsor, IRB, departmental support, and participants.
- Prepare and organize study-related materials as needed.
- Assist feasibility assessment of research protocol including appropriate patient population, budget and specific needs for the study.
Participant Interaction & Support:
- Coordinate study participant visit activities, including scheduling procedures and communicating with participants.
- Assist in educating and supporting participants through study procedures and during study interventions.
- Serve as a liaison between participants and the research team for general study-related questions.
Data Entry & Documentation:
- Maintain and update source documents and submit case report forms (CRFs) as required for clinical trials.
- Collect and enter research data into electronic systems (e.g., REDCap, Epic) and paper records as needed.
- Ensure proper documentation and organization of study records and maintain compliance with institutional and regulatory standards.
- Recognize and report any adverse or serious events to the Principal Investigator.
Administrative & Compliance Assistance:
- Prepare documentation and participate in study monitoring visits, reviews, and audits.
- Support quality assurance activities by reviewing clinical data and ensuring pharmacy compliance with Good Clinical Practice (GCP) and FDA regulations.
- Collaborate with Research Administration, Department Administrators, and the Human Research Protection Program to follow institutional policies.
- Participate in continuing education, research, and training opportunities.
- Support the development of study budgets, contracts, grant applications and study documents for start-up and throughout the lifecycle of the study.
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
- Evening hours may occasionally be required.
- Position is primarily based on-site.
Required Qualifications
Work Experience:
- Four (4) years of experience in health sciences, nursing, medical assisting, biology, or a related field. Relevant education may be substituted for experience on a year-for-year basis.
- One (1) year of clinical research experience.
- Experience with clinical research regulations (FDA, GCP, IRB, HIPAA).
Preferred Qualifications
Certifications: Phlebotomy, RD, Nursing, CMA/AAMA.
Work Experience:
- Clinical research experience related to diabetes, nutrition, physical activity, or weight management.
- Experience with REDCap, Epic, or similar data management systems.
Skills
- Organization
- Communication
- Problem-solving
- Time-management
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
Employee Type:
RegularTime Type:
Full timeRate Type:
SalaryCompensation 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:
$60,800.00 - $91,200.00Minimum
$60,800.00Midpoint
$76,000.00Maximum
$91,200.00
