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Clinical research coordinator resume examples from 2026

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Land interviews using Zippia's AI-powered resume builder.

Updated March 26, 2025
6 min read
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How to write a clinical research coordinator resume

Craft a resume summary statement

A resume summary is your opening statement that highlights your strongest skills and top accomplishments. It is your chance to quickly let recruiters know who you are professionally - and why they should hire you for the clinical research coordinator role.

Step 1: Start with your current job title, or the one you aspire to. Are you a passionate manager? A skilled analyst? It's a good starting point.

Step 2: Next put your years of experience in clinical research coordinator-related roles.

Step 3: Now is the time to put your biggest accomplishment or something you are professionally proud of.

Step 4: Read over what you have written. It should be 2-4 sentences. Your goal is to summarize your experience, not recite your resume.

Hiring managers spend under a minute reviewing resumes on average. This means your summary needs to demonstrate your value quickly and show why you are the perfect fit for the clinical research coordinator position.

Please upload your resume so Zippia’s job hunt AI can draft a summary statement for you.

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List the right project manager skills

Your Skills section is a place to list all relevant skills and abilities. Here is how to make the most of your skills section and make sure you have the right keywords:

  1. Start with the job listing. Frequently, the keywords looked for by recruiters will be listed. Be careful to include all skills in the job listing you have experience with.
  2. Consider all the software and tools you use on a daily basis. When in doubt, list them!
  3. Make sure you use accurate and up to date terms for all the skills listed.
These five steps should give you a strong elevator pitch and land you some clinical research coordinator interviews.

Here are example skills to include in your “Area of Expertise” on a clinical research coordinator resume:

  • Patients
  • Informed Consent
  • IRB
  • Data Collection
  • Research Projects
  • Patient Care
  • GCP
  • Research Data
  • FDA
  • Institutional Review
  • Phlebotomy
  • Data Entry
  • Data Management
  • CRC
  • Excellent Interpersonal
  • Clinical Research Studies
  • Consent Forms
  • HIPAA
  • Regulatory Agencies
  • Vital Signs
  • Federal Regulations
  • Study Procedures
  • Oncology
  • Consent Process
  • Study Subjects
  • Excellent Organizational
  • Clinical Practice
  • Electronic Data
  • ICH
  • Regulatory Binders

Zippia’s AI can customize your resume for you.

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How to structure your work experience

Your employment history is arguably one of the most important parts of your resume. It shows you have experience and foundation in your field to successfully master the clinical research coordinator position. Here is how to most effectively structure your work experience:

  1. List your most recent experience first, followed by earlier roles in reverse chronological order. Employers care about your most recent experience the most.
  2. Start with your job title, company name, city, and state on the left. Align dates in month and year format on the right-hand side.
  3. Include only recent, relevant jobs.

How to write clinical research coordinator experience bullet points

Effective job bullet points do more than just describe your job duties. Instead, they should be specific and measurable accomplishments. Here are some strategies to mastering job bullet points:

  • Use strong action verbs like Led, Built, or Optimized.
  • Follow up with numbers when possible to support your results. How much did performance improve? How much revenue did you drive?
  • Wrap it up by explaining the actions you took to achieve the result and how you made an impact.

Here are examples from great clinical research coordinator resumes:

Work history example #1

Clinical Research Coordinator

American Red Cross

  • Assisted in the development of policies and procedures to improve services and efficiency for patient care.
  • Ensured that ICH/GCP/local regulatory requirements were observed.
  • Managed patient, nursing and research staff education, collaborated with six physicians, and IRB interaction.
  • Produced site-specific advertising materials using Sponsor and IRB-approved language.
  • Researched confidential backgrounds on individuals who attended events with the President and Vice President of the United States.

Work history example #2

Clinical Research Coordinator

NYU Langone Health

  • Selected three investigation sites and principal investigators; obtained Institutional Review Board approval and required FDA documents.
  • Trained CRC's, nurses, and med techs on clinical trials processes and protocol guidelines.
  • Ascertained all FDA and IRB/ WIRB policies are met in relation to the various protocol to my divisions
  • Ensured coordinator and investigator compliance with GCP and ICH guidelines.
  • Expected to play an advanced, expert role in PDS s/PDSS s policies, procedures, processes and other infrastructure developments.

Work history example #3

Nurse Clinician

DaVita

  • Maintained competency with all emergency operational procedures, and initiated CPR and emergency measures, as needed.
  • Assessed patient and family learning readiness and educated patient accordingly.
  • Attended monthly Facility Administrator meetings.
  • Analyzed assessment and lab data, brought concerns to the attention of physician.
  • Provided hospice education and counseling.

Work history example #4

Office Nurse

DaVita

  • Maintained competency with all emergency operational procedures, and initiated CPR and emergency measures, as needed.
  • Learned and applied learning while working in hospital departments of emergency medicine and medical surgical floor.
  • Certified in ACLS, Stroke Team and BLS.
  • Started as a patient flow nurse (rooming, vitals, assisting with procedures/occasionally filling in for the triage dept).
  • Provided personalized telephone advice and triage for pediatric and adult patients.

Zippia’s AI can customize your resume for you.

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Add an education section to your resume

Here is the best way to format your education section:

  • Display your highest degree first.
  • If you graduated over 5 years ago, put this section at the bottom of your resume. If you lack relevant work experience, the education section should go to the top.
  • If you have a bachelor's or master's degree, do not list your high school education.
  • If your graduation year is more than 15-20 years ago, it's better not to include dates in this section.

Here are some examples of good education entries from clinical research coordinator resumes:

Bachelor's Degree in psychology

New York University, New York, NY

2008 - 2011

Highlight your clinical research coordinator certifications on your resume

Certifications can be a crucial part of your resume. Many jobs have required certifications.

Start simple. Include the full name of the certification. It's also good to mention the organization that issued the certification. Next, specify when you obtained the certification.

Here are some of the best certifications to have on clinical research coordinator resumes:

  1. Certified Clinical Research Professional (CCRP)
  2. Certified Clinical Research Coordinator (CCRC)
  3. Certified Phlebotomy Technician (CPT)
  4. Certified Clinical Research Associate (CCRA)
  5. Clinical Trial Investigator (CTI)
  6. Certified Clinical Medical Assistant (NHA)
  7. Registered Medical Assistant
  8. Professional Researcher Certification (PRC)
  9. Nationally Certified Medical Assistant (NCMA)

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