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Clinical Research Coordinator resume template

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Built for

  • ✓CRCs managing multiple concurrent industry or academic trials
  • ✓Research assistants stepping up to coordinator roles
  • ✓Coordinators listing ACRP/SOCRA certification and EDC systems

What you get

  • ✓Live on-page editing — click any text and type, paginated like the final PDF
  • ✓Selectable-text PDF export with clickable email and portfolio links
  • ✓AI import: upload your old resume PDF and land in this template, editable
  • ✓Scored 96/100 — interview-ready against the 30 published rules, measured by exporting this exact template. Certified: we only badge templates at 90 or above, a stricter bar than the 85 our checker calls interview-ready, so the design leaves headroom for your own content.
Steven Hobbs
Clinical Research Coordinator
steven.hobbs@example.com
(555) 641-7823
Ann Arbor, MI
linkedin.com/in/stevenhobbs
Summary

ACRP-certified research coordinator with seven years running Phase II-III trials in cardiology and vaccines. Manages six concurrent studies with 140 enrolled participants and hits 96% of enrollment targets.

Experience
Clinical Research Coordinator II — Great Lakes Clinical Research
2022 – Present
  • Coordinate 6 concurrent Phase II-III cardiology trials with 140 enrolled participants across two sites
  • Hit 96% of enrollment targets on the last four studies through EMR-based pre-screening
  • Closed 100% of monitoring-visit action items within 10 business days across 22 sponsor visits
Clinical Research Coordinator — Arbor Point Research Group
2020 – 2022
  • Managed 4 vaccine and metabolic studies end-to-end, screening 300+ candidates yearly
  • Kept source-to-EDC entry within 48 hours across 5,000+ data points at a 0.4% query rate
Clinical Research Assistant — Riverwalk Cardiology Group
2019 – 2020
  • Supported two device registries, completing 400 follow-up visits and case report forms annually
  • Processed, centrifuged, and shipped 30 biospecimen kits weekly with zero temperature excursions
Education
B.S. Biology — Eastern Michigan University2019
Skills
  • Participant recruitment & consent
  • IRB submissions
  • GCP / ICH E6
  • Adverse event reporting
  • Biospecimen handling (IATA)
  • Medidata Rave
  • REDCap
  • Epic
  • CTMS
  • eRegulatory binders
Certifications
CCRC - Certified Clinical Research Coordinator (ACRP)
GCP certification (CITI Program)

Frequently asked questions

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Will my PDF have selectable text for ATS systems?

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Can I switch templates without retyping anything?

Yes — your content and the design are stored separately, so switching templates re-flows the same content instantly and losslessly. Try every one of them.

Should I name the studies or sponsors I've worked on?

Name therapeutic areas and phases, not protocol numbers or unannounced sponsors — confidentiality agreements usually cover those. 'Six Phase II-III cardiology trials' is specific enough to impress and safe to print.

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