Clinical Research Coordinator Resume Template

Writing the Clinical Research Coordinator Resume

Create Resume

Submitting a resume is the best chance you will get to stand out. In today’s competitive atmosphere, the best jobs are easier to get when your skills are highlighted by a powerful resume. A well-structured Clinical Research Coordinator resume template like the one below will give you the edge you need.

Resume Template for a Clinical Research Coordinator

Katherine Johnson

Professional Summary

Adaptive Clinical Research Coordinator skilled in multi-team management works with physicians and medical staff to correlate hospital procedure with clinical trials, and reports to medical personnel during off-site research trials. Proven experience with regulations regarding research projects. Produces accurate documents, reports while maintaining a compassionate relation to study participants.

Core Qualifications

• Access, Microsoft Office
• Regulation compliance
• FDA and IRB regulations
• Phlebotomy


Clinical Research Coordinator II, July 2013 – present
Ann & Robert Lurie Children’s Hospital of Chicago – Chicago, Illinois

• Updated case reports and source documents for clinical trials, arranged study interviews, and recruitment
• Updated medical records, maintained information on protocol and case reports for each trial, developed flow sheets and identified subject eligibility
• Performed QA/QC procedures, worksheets and study materials, collected data and ordered supplies
• Prepared consent amendments and processed specimens
• Prepared sponsor files for FDA compliance and GCP guidelines

Clinical Research Coordinator, May 2010 – July 2013
Evanston Premier Healthcare Research – Evanston, Illinois

• Recruited and interviewed study participants
• Arranged patient visits
• Created source documents, maintained reports and met with monitors on routine site visits
• Conducted clinical Phase II through IV trials for the Multispecialty site

Clinical Research, July 2008 – May 2010
NorthShore University – Evanston, Illinois

• Collaborated with sponsors/CROs to create IRB submissions, revisions and consent material
• Submitted applications and revisions for research and studies, made amendments to proposals and weekly progress reports
• Reported on progress of research programs to IRB
• Developed brochures that outlined protocol and recruitment information for specific studies
• Collected data on research progress, adverse reactions, deviations and results
• Summarized research trials for the Administrative Director, IRB and Board of Directors
• Ensured regulatory compliance
• Maintained trial policy records and procedure materials


2008, Associate of Science in Clinical Research Coordinator (CRC)
Mayo Clinic College of Medicine/University of Minnesota – Rochester, Minnesota

Customize Resume