Clinical Research Coordinator II — Study Operations & IRB Support

WakeMed; Raleigh (NC); On-site; USD 52,000 - 78,000; Full time

Job summary

WakeMed Health & Hospitals in Raleigh is seeking a Research Coordinator II to assist the research team in planning and implementing clinical studies, including subject recruitment, consent, follow-up, and data collection.

The role covers monitoring visits, IRB submissions, and reviews of research billing, with responsibilities to report adverse events and protocol deviations and to train new staff and learners.

Qualifications

• Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) required.
• 2 years direct experience in a clinical research role required.

Responsibilities

• Assist planning and implementation of clinical research studies.
• Recruit and consent subjects; conduct follow-up and CRF completion.
• Coordinate monitoring visits and IRB submissions.
• Conduct research billing reviews; report adverse events and protocol deviations.
• Provide training or guidance to new research staff, interns, medical students or other learners.

Education

High School Diploma or Equivalent

Job description

WakeMed Health & Hospitals in Raleigh is seeking a Research Coordinator II to assist the research team in planning and implementing clinical studies, including subject recruitment, consent, follow-up, and data collection.

The role covers monitoring visits, IRB submissions, and reviews of research billing, with responsibilities to report adverse events and protocol deviations and to train new staff and learners.