Clinical Research Coordinator - Pulmonary/CC Sleep (OnSite)

University of Kansas Medical Center; Kansas City (KS); On-site; USD 61,000 - 91,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Paid time off and holidays

Retirement plan (457/403b)

Employer-paid life insurance and long‑

Discretionary day after six months

Job summary

University of Kansas Medical Center in the Kansas City metro area seeks a Clinical Research Coordinator in Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine) to coordinate and manage multiple clinical studies, ensure regulatory compliance, and support investigators and sponsors.

The role includes developing study documents, screening and enrolling participants, obtaining informed consent, collecting data, and coordinating submissions to IRB and regulatory bodies.

Qualifications

• Four (4) years of experience in health sciences, nursing, biology, or related field; education may substitute on a year-for-year basis.
• Two (2) years of clinical research experience.
• Experience with clinical research regulations (FDA, GCP, IRB, HIPAA).

Responsibilities

• Coordinate multiple clinical research studies, including investigator-initiated and industry-sponsored trials.
• Develop and maintain study documents, including regulatory binders and CRFs.
• Identify and screen eligible participants; obtain informed consent and schedule visits.
• Collect data, ensure regulatory compliance, and assist with audits and regulatory submissions.
• Coordinate sample collection and collaborate with investigators and sponsors.

Skills

Regulatory compliance

Study coordination

Participant recruitment

Data management

Communication skills

Education

Bachelor's degree in health sciences or related field

Tools

REDCap

Epic

Job description

University of Kansas Medical Center in the Kansas City metro area seeks a Clinical Research Coordinator in Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine) to coordinate and manage multiple clinical studies, ensure regulatory compliance, and support investigators and sponsors.

The role includes developing study documents, screening and enrolling participants, obtaining informed consent, collecting data, and coordinating submissions to IRB and regulatory bodies.