Skip to main content

Science & Research

Clinical Research Coordinator Resume Example

A clinical research coordinator resume must show ATS systems and study sponsors that you can manage IRB compliance, patient recruitment, and data integrity across multiple concurrent trials.

Build My Clinical Research Coordinator ResumeCheck My ATS Score

Clinical Research Coordinator Resume Sample

A complete, recruiter-approved example you can use as a starting point. Open it in the builder to edit every line.

MARISOL TORRES

Clinical Research Coordinator II

Rochester, MN · m.torres@email.com · (555) 762-4413

Summary

Clinical research coordinator with 6 years managing Phase I-III oncology and cardiology trials from IRB submission through close-out. Recruited over 300 participants and maintained a zero major-finding audit record across 5 sponsor inspections.

Experience

Clinical Research Coordinator II · Mayo Clinic

2021 - Present

  • Coordinate 6 concurrent Phase II/III oncology trials, managing IRB submissions and protocol amendments for each
  • Recruited and consented 180+ participants over 3 years, exceeding enrollment targets by an average of 18%
  • Maintained a zero major-finding record across 5 sponsor and FDA audits by enforcing strict source-document verification

Clinical Research Coordinator I · Parexel International

2018 - 2021

  • Managed regulatory documentation and CRF completion for 4 cardiology device trials across 2 sites
  • Reduced query resolution time by 30% by implementing a weekly EDC discrepancy-review process

Education

B.S. Biology — University of Minnesota · 2018

Skills

GCP, IRB Submissions, Informed Consent, Medidata Rave, REDCap, Adverse Event Reporting, Protocol Adherence, CTMS, Patient Recruitment, Regulatory Compliance, Source Document Verification

Use This Example in the Builder

Must-Have Keywords for Clinical Research Coordinator Resumes

These are the keywords ATS systems and recruiters search for. Include them naturally in your Skills, Summary, and Experience sections.

IRB SubmissionsGCPInformed ConsentPatient RecruitmentCRFProtocol AdherenceAdverse Event ReportingCTMSRegulatory ComplianceData AbstractionSite MonitoringEDC Systems

The Right Resume Structure for Clinical Research Coordinator Roles

ATS systems parse your resume top to bottom. The order of your sections matters — here is the order that works best for Clinical Research Coordinator applications:

  1. 1Contact Information
  2. 2Professional Summary
  3. 3Core Competencies
  4. 4Professional Experience
  5. 5Education
  6. 6Certifications

ATS Optimization Tips for Clinical Research Coordinator Resumes

  • Name-drop the trial phases you've supported (Phase I-IV) — sponsors filter for this specifically.
  • Quantify enrollment numbers: "Recruited and consented 85 participants across 3 concurrent trials" shows capacity.
  • Highlight GCP certification and IRB/regulatory submission experience in your top third.
  • List EDC/CTMS platforms by name (Medidata Rave, Veeva, REDCap) since sponsors search for specific systems.
  • Show audit performance: "Zero major findings across 4 FDA/sponsor audits" is a powerful trust signal.
  • Emphasize patient-facing skills alongside data skills — this role bridges clinical care and research rigor.
  • Include therapeutic area experience (oncology, cardiology, etc.) to match sponsor-specific searches.

Ready to Build Your Clinical Research Coordinator Resume?

Start from this pre-filled Clinical Research Coordinator example — it already has the right keywords, format, and structure. Edit every line in the builder.

Start Building FreeBrowse All Examples

Related Resume Examples

Research Associate Resume →Epidemiologist Resume →Microbiologist Resume →Research Scientist Resume →View all examples →