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Resume Template for a Clinical Research Coordinator
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.
• Access, Microsoft Office • Regulation compliance • FDA and IRB regulations • GCP AND CCRC • 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