Clinical Research Coordinator - Internal Medicine (Diabetes Institute)

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:
Regular

Time Type:
Full time

Rate Type:
Salary

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: $60,800.00 - $91,200.00

Minimum
$60,800.00

Midpoint
$76,000.00

Maximum
$91,200.00

Application Instructions:
To learn more and apply online, please visit https://kumc.wd5.myworkdayjobs.com/en-US/kumc-jobs/job/Kansas-City-Metro-Area/Clinical-Research-Coordinator---Internal-Medicine--Diabetes-Institute-_JR010563 or go to https://careers.kumc.edu/ and search for position number JR010563.

Applications must be submitted directly through the KU Medical Center website to be considered for this position. Any applications submitted via email or this website will NOT be reviewed or considered.

About KU Medical Center:
The University of Kansas Medical Center's mission is to educate exceptional health care professionals through a full range of undergraduate, graduate, professional, postdoctoral and continuing education programs in the schools of Medicine, Nursing and Health Professions. KU Medical Center also advances the health sciences through world-class research programs; provides compassionate and state-of-the-art patient care in an academic medical center environment; and works with communities in every Kansas county to improve the health of Kansans. Learn more at www.kumc.edu.

Benefits:
KUMC offers a range of great benefits that support employees and eligible family members. Our health insurance benefits begin on hire date and KUMC offers other exciting benefits such as paid parental leave, generous employer retirement contributions and other resources to improve health and well-being. For more information, please visit https://www.kumc.edu/human-resources/benefits.html

Equal Employment Opportunity Statement

The University of Kansas Medical Center is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, national origin, ethnicity, ancestry, age, protected veteran or disability status, marital status, parental status, or genetic information. http://policy.ku.edu/IOA/nondiscrimination">http://policy.ku.edu/IOA/nondiscrimination

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