Pulmonary, Critical Care & Sleep CRC

University of Kansas Medical Center; United States; On-site; USD 61,000 - 91,000; Full time

Benefits offered by this job

Comprehensive benefits package

On-site work

Job summary

The University of Kansas Medical Center is seeking a Clinical Research Coordinator in the Division of Pulmonary, Critical Care, and Sleep Medicine to coordinate and manage clinical studies in accordance with regulatory requirements and institutional policies.

The role involves study planning, recruitment, data collection, and regulatory submissions, with on-site responsibilities and collaboration with investigators and sponsors.

Qualifications

• Four (4) years of clinical research experience or health sciences background.
• Experience with FDA, GCP, IRB, and HIPAA regulations.
• Strong written and verbal communication, organization, and problem-solving skills.
• Proficiency with data management systems (REDCap, Epic) is preferred.

Responsibilities

• Coordinate multiple clinical research studies, including investigator-initiated and industry-sponsored trials.
• Develop and maintain study documents such as regulatory binders and CRFs.
• Ensure compliance with IRB, FDA, NIH, and institutional regulations.
• Recruit, screen, consent, and follow study participants; schedule visits.
• Collect data, manage EDC entries, and prepare regulatory submissions.
• Collaborate with investigators, sponsors, and healthcare providers; train staff.

Job description

The University of Kansas Medical Center is seeking a Clinical Research Coordinator in the Division of Pulmonary, Critical Care, and Sleep Medicine to coordinate and manage clinical studies in accordance with regulatory requirements and institutional policies.

The role involves study planning, recruitment, data collection, and regulatory submissions, with on-site responsibilities and collaboration with investigators and sponsors.