CLINICAL RESEARCH COORDINATOR

Duke CareersDurham, NC

About The Position

Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more than 6,000 staff, the Duke University School of Medicine along with the Duke University School of Nursing, Duke University Health System and the Private Diagnostic Clinic (PDC) comprise Duke Health. a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Primary Care, Duke Home and Hospice, Duke Health and Wellness, and multiple affiliations. Be You. Be Bold. Choose Duke. Be You. At Duke, we celebrate individuality and the unique perspectives that each member of our community brings. As a Clinical Research Coordinator, you’ll be a vital part of a collaborative, interdisciplinary team supporting cutting-edgemovement disorders research while ensuring the highest standards of ethics, data integrity, and participant care. Be Bold. You will take ownership of complex clinical research activities and help advance innovative science.

Requirements

  • Completion of an Associate’s degree is required.
  • A minimum of two years of relevant clinical or research experience is required.
  • Completion of the DOCR North Carolina state‑approved Clinical Research Apprenticeship Program may substitute for one year of the required experience.

Nice To Haves

  • Relevant research training or certifications are preferred and may be considered toward experience equivalency.

Responsibilities

  • Coordinate and manage complex clinical research studies, including regulatory submissions, study documentation, and protocol execution.
  • Serve as a primary liaison with sponsors, CROs, IDS, and internal stakeholders.
  • Ensure compliance with IRB, FDA, institutional, and sponsor requirements.
  • Manage investigational products, participant recruitment, retention, and study visits.
  • Collect, manage, and ensure quality and security of clinical research data.
  • Support audits, monitoring visits, and study closeout activities.
  • Contribute to scientific advancement through literature reviews, publications, and presentations.

Benefits

  • Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members.

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume

What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

Associate degree

Number of Employees

101-250 employees

© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service