Resume Example
Clinical Research Coordinator Resume Example
Show protocol adherence, IRB coordination, and data integrity. This sample focuses on compliant trial delivery.
Classic Professional
Traditional single-column ATS-optimized layout. Best for conservative industries.
Keywords
Sample bullets
- Coordinated 15 active trials with 100% protocol compliance and zero audit findings.
- Improved enrollment rate by 20% by refining screening workflows.
- Submitted IRB amendments and SAE reports within required timelines.
Soft skills
- Organization
- Attention to detail
- Patient communication
- Regulatory discipline
Certifications
- ACRP-CP
- SOCRA CCRP
Why this works
- Highlights compliance and audit readiness.
- Shows enrollment and retention impact.
- Demonstrates cross-functional coordination.
Step-by-Step Guide
How to Write a Clinical Research Coordinator Resume
Highlight Research Experience
Feature experience with clinical trial phases, therapeutic areas, and study types. Include number of studies coordinated and enrollment achievements.
Showcase Regulatory Knowledge
Demonstrate understanding of ICH-GCP, FDA regulations, IRB submissions, and informed consent. Include experience with audits and inspections.
Demonstrate Protocol Execution
Show experience with subject recruitment, screening, enrollment, and follow-up visits. Include data collection, adverse event reporting, and query resolution.
Quantify Enrollment and Compliance
Use metrics like enrollment numbers, retention rates, protocol deviations, and query response times. Show ability to meet study timelines.
Include Technology and Certification
Highlight EDC systems (Medidata, Veeva), CCRC or CCRP certification, and therapeutic area specialization (oncology, cardiology, CNS).
Summary Examples
Good vs. Bad Resume Summaries
“CCRC-certified Clinical Research Coordinator with 5 years coordinating Phase II-IV oncology trials. Enrolled 300+ subjects across 15 studies with 92% retention rate. Zero FDA 483 observations. Expert in Medidata Rave and Veeva CTMS.”
Shows certification, therapeutic area, enrollment success, compliance record, and systems.
“Clinical Research Coordinator specializing in cardiovascular and metabolic trials with 6 years experience. Led first-in-human study with 100% protocol compliance. Reduced screen failure rate by 30% through pre-screening optimization. Trained 10 new coordinators.”
Specialty focus, protocol compliance, efficiency improvement, leadership role.
“Research coordinator with experience in clinical trials. Familiar with IRB submissions and data collection.”
Too generic, no metrics, doesn't show therapeutic area or trial phase experience.
“Looking for CRC position. Completed GCP training and interested in clinical research.”
GCP training is baseline requirement, no experience demonstrated.
Action Verbs
Power Words for Clinical Research Coordinator Resumes
Common Mistakes
What to Avoid
- ✗Not specifying trial phases and therapeutic areas
- ✗Missing enrollment numbers and retention rates
- ✗Omitting regulatory compliance and audit experience
- ✗Being vague about EDC and CTMS systems
- ✗Not showing certification (CCRC, CCRP)
- ✗Missing protocol deviation and query metrics
Salary ranges
| Level | US | EU | Canada |
|---|---|---|---|
| Entry | USD 50,000-65,000 | EUR 34,500-44,800 | CAD 58,000-75,400 |
| Mid | USD 65,000-80,000 | EUR 44,800-55,100 | CAD 75,400-92,800 |
| Senior | USD 80,000-95,000 | EUR 55,100-65,500 | CAD 92,800-110,100 |
Market themes
- Academic medical centers and pharma-sponsored trials pay premiums
US hot markets
- Boston
- San Francisco
- New York
- San Diego
- Chicago
EU hot markets
- London
- Dublin
- Amsterdam
Canada hot markets
- Toronto
- Vancouver
- Montreal
FAQ
Common questions about this role
What should clinical research coordinators emphasize?
Protocol compliance, data integrity, and IRB documentation.
Which tools should be listed?
REDCap, CTMS platforms, and GCP documentation tools.
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