Clinical Research Coordinator - Pulmonary & Sleep Med

The University of Kansas Health System; Kansas City (MO); On-site; USD 61,000 - 91,000; Full time

Benefits offered by this job

Comprehensive benefits

Paid time off

Retirement plan

On-site work

Job summary

The University of Kansas Health System is seeking a Clinical Research Coordinator in Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine) to coordinate and manage clinical studies in accordance with regulatory standards. You will oversee recruitment, consent, data collection, and reporting in collaboration with investigators and sponsors.

Responsibilities include study coordination, regulatory documentation, patient enrollment, data management, and ensuring adherence to FDA, GCP,

Qualifications

• Four (4) years of experience in health sciences, nursing, biology, or related field.
• Two (2) years of clinical research experience.
• Experience with clinical research regulations (FDA, GCP, IRB, HIPAA).
• Phlebotomy certification preferred.
• Experience with REDCap, Epic, or similar data management systems.

Responsibilities

• Coordinate multiple clinical research studies, including investigator-initiated and industry-sponsored trials.
• Develop and maintain study documents, including regulatory binders, case report forms, and data collection tools.
• Ensure protocols are conducted in accordance with IRB, FDA, NIH, and institutional regulations.
• Monitor study progress and adherence to timelines.
• Identify eligible participants and obtain informed consent.
• Collect and enter data into EDC systems; ensure data quality and regulatory compliance.
• Coordinate sample collection and handling; assist with procedures (e.g., pulmonary function tests, sleep studies).
• Act as liaison between sponsors, investigators, patients, and healthcare providers.

Skills

Organization

Problem-solving

Communication

Computer skills

Tools

REDCap

Epic

Job description

The University of Kansas Health System is seeking a Clinical Research Coordinator in Internal Medicine (Pulmonary, Critical Care, and Sleep Medicine) to coordinate and manage clinical studies in accordance with regulatory standards. You will oversee recruitment, consent, data collection, and reporting in collaboration with investigators and sponsors.

Responsibilities include study coordination, regulatory documentation, patient enrollment, data management, and ensuring adherence to FDA, GCP,