Back to All Templates
    Medicine
    ATS-Friendly
    One-Page

    Clinical Research Coordinator Resume Template - ATS Friendly

    This is a ready-to-use one-page resume template for a Clinical Research Coordinator. It is designed to be ATS-friendly with clear section headings, simple formatting, and keyword-rich content tailored for medicine and clinical research roles. Dummy data demonstrates how to present name, contact details, profile, experience, skills, certifications, and education in a concise, professional layout.

    Keywords:

    clinical research coordinator resume template
    ats resume template
    one page resume
    gcp resume
    clinical trials coordinator CV
    medical resume template
    research coordinator resume
    CRP resume sample
    Template Preview
    Priya Kapoor, MSc
    Clinical Research Coordinator | GCP | Trial Operations | Data Integrity
    Email: Priya.Kapoor@example.com
    Phone: +1 555-012-3456
    LinkedIn: linkedin.com/in/priyakapoor
    ResearchGate: researchgate.net/profile/Priya_Kapoor

    Profile Summary

    Accomplished clinical research coordinator with 5+ years coordinating Phase I-IV trials across oncology and infectious diseases. Demonstrates strong patient engagement, site management, and regulatory compliance (ICH-GCP). Proven track record in achieving timely milestones, improving data quality, and ensuring patient safety.

    Experience

    Global Health Trials, Inc. — Clinical Research Coordinator
    New York, NY · Mar 2021 - Present
    • Led end-to-end coordination for 12+ trials across oncology and infectious diseases; ensured 98% on-time milestones.
    • Implemented centralized EDC data checks reducing data queries by 28% and improving query resolution time by 32%.
    • Managed site start-up activities, patient recruitment strategies, and informed consent processes with a focus on diversity and inclusion.
    • Supervised a team of 4 site coordinators; delivered quarterly training on ADR reporting and SAE documentation.
    UrbanMed Research Partners — Clinical Trial Administrator
    Boston, MA · Jun 2018 - Feb 2021
    • Supported multi-site trials, ensured regulatory compliance, and maintained trial master file (TMF) readiness.
    • Coordinated patient screening, enrollment, and retention strategies increasing enrollment by 22% year over year.
    • Collaborated with data managers to resolve data discrepancies and prepare monitoring visit packets.

    Skills

    • Regulatory Compliance (ICH-GCP)
    • EDC & CTMS (eClinicalWorks, Medidata)
    • Study Start-Up & TMF Management
    • Informed Consent & Patient Safety
    • SAE/AE Reporting
    • Data Cleaning & CRF Design
    • Site Training & Team Leadership
    • Patient Recruitment & Retention

    Certifications

    • Good Clinical Practice (GCP) Certification
    • ICH-GCP Certification
    • Certification in Clinical Research (CCR)

    Education

    Master of Science in Clinical Research
    Columbia University, New York, NY · 2018 - 2020
    Bachelor of Science in Biology
    University of Mumbai, Mumbai, India · 2012 - 2016

    How to Use This Template

    1. Click the "Download this template" button below the preview
    2. Open the downloaded HTML file in your web browser
    3. Right-click on the resume preview and select "Print" or press Ctrl+P (Cmd+P on Mac)
    4. Choose "Save as PDF" as your printer destination
    5. Edit the PDF with your own information using any PDF editor
    6. Alternatively, copy the content and paste into Microsoft Word or Google Docs for easier editing

    💡 Pro Tips:

    • • Replace all placeholder text with your actual information
    • • Keep the formatting simple and ATS-friendly
    • • Use relevant keywords from the job description
    • • Keep your resume to one page for optimal ATS scanning
    Browse More Templates