Clinical Research Coordinator

University of Kansas Medical Center Kansas City, KS Full-time Research

Posted on April 2, 2024

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Clinical Research Coordinator

Department:
SOM KC Division of Cardiovascular Diseases
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CCR

Position Title:
Clinical Research Coordinator

Job Family Group:
Professional Staff

Job Description Summary:
This position is responsible for working collaboratively with multidisciplinary teams, research and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research. The Clinical Research Coordinator will manage clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data. Monitor participants' progress including documenting and reporting adverse events. Participate in periodic quality assurance audits of protocols.

Job Description:

Required Qualifications

Education: Associate's degree, OR an equivalent combination of education and relevant work experience equaling two (2) years.

Work Experience:

Two (2) years prior research or related experience.
Experience with regulations governing clinical research (CFR, GCP, HIPAA).
Experience with study budgets, contracts and grant applications.
Presentation experience.

Preferred Qualifications

Education: RN or BSN.

Work Experience:

Cardiovascular research experience.
Three (3) years or more research experience.
Experience using medical terminology.
Experience working with diverse populations.

Skills:

Detail oriented
Interpersonal communication skills.
Organizational and communication skills.

Job Duties Outlined

Under the direction of the Principal Investigator, recruit and educate potential patients and evaluate potential patient eligibility for clinical trials.
Assesses feasibility of research protocol, including appropriate patient population, budget and specific needs for the study.
Maintain source documents and submit case report forms (CRFs) as required for clinical trials. Completes and corrects case report forms, ensuring accuracy of all records connected with each study with attention to medical events and concomitant medications as well as documentation for each study related event.
Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors.
Perform study procedures as outlined in the protocol and within state and institutional scope of practice.
Maintains current KURI-required education, i.e. Human Subjects Protection, HIPAA, Adheres to GCP guidelines.
Assist clinical staff with phlebotomy and sample collection, processing, handling, and shipping as outlined in the protocol and within institutional/KUMC policy.
Monitors awarded grants and contracts for compliance with performance, reporting and accounting requirements.
Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment, supplies and study participants.
Prepare documentation and participate in study monitoring visits, reviews and audits. Provide written and verbal reports to Principal Investigator and Research Operations Manager as required.
Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria, and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR.
Work closely with the Research Institute and Human Research Protection Program and have a working knowledge of KUMC policies and procedures.
Attends all staff meetings as well as meetings both onsite and off-site as required by study. Serves as mentor for new staff members.
Attend continuing education, research and training seminars as requested by manager.
Other relevant duties as requested by the supervisor.

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 nine 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:
$58,000.00 - $86,000.00
Minimum
$58,000.00
Midpoint
$72,000.00
Maximum
$86,000.00

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_JR006866 or go to https://careers.kumc.edu/ and search for position number JR006866.

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

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Clinical Research Coordinator

University of Kansas Medical Center

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