Pulmonary & Critical Care Clinical Research Coordinator II

Duke University

Durham (NC)

On-site

USD 61,000 - 102,000

Full time

6 days ago
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Job summary

Duke University School of Medicine is seeking a Clinical Research Coordinator II to support pulmonary and critical care studies, from participant recruitment through study closeout. You will work with investigators, research participants, sponsors, and multidisciplinary teams to ensure safety, efficiency, and regulatory compliance.

The role requires coordinating complex studies, IRB submissions, and managing data and biospecimens, with opportunities to contribute to grants and publications.

Qualifications

  • Associate's degree completed.
  • Two years of relevant research experience required.
  • IRB submissions and regulatory compliance experience preferred.
  • Experience handling biospecimens and lab documentation is a plus.

Responsibilities

  • Coordinate and manage pulmonary and critical care clinical research studies.
  • Recruit, screen, consent, enroll, and retain research participants.
  • Schedule and conduct study visits while ensuring protocol compliance.
  • Collect, enter, review, and maintain research data and study documentation.
  • Process, track, and maintain human biospecimens and laboratory records.
  • Prepare IRB applications and regulatory documents; support sponsor communications.
  • Utilize OnCore, REDCap, and Epic/Maestro Care to manage study activities.
  • Collaborate with investigators and teams to support grants, presentations, and publications.

Skills

Microsoft Office
Internet browsers

Education

Associate's degree

Tools

OnCore
REDCap
Epic/Maestro Care

Job description

Duke University School of Medicine is seeking a Clinical Research Coordinator II to support pulmonary and critical care studies, from participant recruitment through study closeout. You will work with investigators, research participants, sponsors, and multidisciplinary teams to ensure safety, efficiency, and regulatory compliance.

The role requires coordinating complex studies, IRB submissions, and managing data and biospecimens, with opportunities to contribute to grants and publications.

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