Management

Clinical Research Coordinator Resume Example

Professional resume template and tips for Clinical Research Coordinator positions

Clinical Research CoordinatorClinical Program ManagerClinical Project ManagerClinical Research AdministratorClinical Research ManagerResearch CoordinatorClinical CoordinatorClinical Data Coordinator

If you're pursuing a career as a Clinical Research Coordinator, this guide provides the specific roadmap you need. You'll discover the core daily tasks, from subject scheduling to protocol procedures, and the exact technical tools, like clinical trial management software and SAS, required to manage projects effectively. We detail the essential blend of soft skills—such as critical thinking and personnel management—and foundational knowledge areas for success. This comprehensive overview equips you with the insights to understand the role deeply and build a compelling application. Use this resource to refine your expertise and prepare a standout Clinical Research Coordinator resume with Mokaru.

TYLER HALL

Clinical Research Coordinator
tyler.hall@email.com | +1 (555) 123-4567 | San Francisco, CA

Professional Summary

Clinical Research Coordinator with 8+ years of experience managing Phase II-IV oncology and cardiovascular trials. Streamlined participant enrollment for a multi-site study, accelerating recruitment by 30% against target. Proficient in full protocol lifecycle coordination, from screening to data collection, utilizing EDC systems and SPSS for analysis.

Skills

Technical Skills: Microsoft Excel, Microsoft Office software, Microsoft PowerPoint, Microsoft Word, Microsoft Access, IBM SPSS Statistics
Soft Skills: Reading Comprehension, Active Listening, Writing, Speaking, Coordination

Experience

Lead Clinical Research Coordinator
2022 - Present
Nexus Clinical Trials Management
  • Led protocol development and strategic planning for a multi-center Phase III trial, leveraging critical thinking and coordination to accelerate regulatory approval by 20%
  • Directed cross-functional team training on complex protocol procedures using Microsoft PowerPoint, improving team compliance and reducing protocol deviations by 15%
  • Implemented a comprehensive subject monitoring system using Microsoft Access, enhancing social perceptiveness in adverse event tracking and improving data quality by 25%
Clinical Research Coordinator II
2019 - 2022
Apex Research Solutions Group
  • Managed all aspects of patient scheduling and data collection for a 150-subject study, utilizing Microsoft Excel to coordinate appointments and maintain 98% protocol adherence
  • Authored and submitted all institutional review board documentation and progress reports, applying strong writing skills to secure timely approvals with zero major revisions
  • Performed statistical analysis of preliminary data using IBM SPSS Statistics, presenting findings that supported a key protocol amendment and improved subject retention
Associate Clinical Research Coordinator
2016 - 2019
Veritas Clinical Management Partners
  • Screened over 200 potential subjects through medical record reviews and interviews, applying active listening to accurately assess eligibility against strict protocol criteria
  • Prepared all study-related documentation and worksheets under senior supervision, utilizing Microsoft Word to ensure consistency and support regulatory audit readiness
  • Conducted patient interviews and performed protocol procedures like vital signs, applying reading comprehension to precisely execute tasks and maintain data integrity

Education

Bachelor of Science
2011 - 2015
State University

Certificates

  • Certified Clinical Research Professional (CCRP)
  • Project Management Professional (PMP)
  • Human Subjects Research (HSR) Certification

Build Your Clinical Research Coordinator Resume

Create a professional, ATS-optimized resume tailored for Clinical Research Coordinator positions in minutes.

Create Free Resume

What does a Clinical Research Coordinator do?

A Clinical Research Coordinator performs various tasks on a daily basis. Here are the core responsibilities you can expect in this role:

  • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
  • Inform patients or caregivers about study aspects and outcomes to be expected.

What skills do you need as a Clinical Research Coordinator?

Employers hiring for Clinical Research Coordinator positions look for candidates with a strong combination of technical and soft skills. Here are the most important skills to highlight on your resume:

Microsoft Excel
Microsoft Office software
Microsoft PowerPoint
Microsoft Word
Microsoft Access
IBM SPSS Statistics
SAS
The MathWorks MATLAB
Microsoft Project
Python

What knowledge areas are important for a Clinical Research Coordinator?

Beyond skills and tools, employers value candidates with deep knowledge in these areas. Consider highlighting relevant coursework, certifications, or experience:

Customer and Personal ServiceEnglish LanguageAdministrativeMedicine and DentistryAdministration and ManagementBiologyComputers and ElectronicsMathematicsEducation and TrainingPublic Safety and Security

How do I write a great Clinical Research Coordinator resume?

Creating an effective Clinical Research Coordinator resume requires focusing on what employers in the Management sector value most.

Use relevant keywords

ATS systems scan for specific terms. Include these keywords naturally throughout your resume:

WritingSpeakingMicrosoft WordMicrosoft ExcelActive ListeningMicrosoft PowerPointReading ComprehensionMicrosoft Office software

Quantify your impact

When describing how you "schedule subjects for appointments, procedures, or inpatient stays as required by study protocols", include metrics like percentages, team sizes, budgets, or project scope to demonstrate real results.

Showcase technical proficiency

Highlight hands-on experience with Microsoft Excel, Microsoft Office software, Microsoft PowerPoint and any customer and personal service certifications that validate your expertise.

Match the experience level

For Clinical Research Coordinator roles, employers typically expect usually requires a 4-year bachelor's degree. Highlight matching qualifications prominently at the top of your resume.

Example bullet points

Here are some strong bullet points you could adapt for your Clinical Research Coordinator resume:

  • Led protocol development and strategic planning for a multi-center Phase III trial, leveraging critical thinking and coordination to accelerate regulatory approval by 20%
  • Directed cross-functional team training on complex protocol procedures using Microsoft PowerPoint, improving team compliance and reducing protocol deviations by 15%
  • Implemented a comprehensive subject monitoring system using Microsoft Access, enhancing social perceptiveness in adverse event tracking and improving data quality by 25%

How to use AI to improve your Clinical Research Coordinator resume

AI tools like ChatGPT can be incredibly helpful when crafting your Clinical Research Coordinator resume. They can help you brainstorm achievements, rephrase bullet points for impact, identify missing keywords, and tailor your content to specific job descriptions.

However, AI is not perfect. Always proofread the output carefully. AI can sometimes make factual errors, use generic language, or miss the nuances of your specific experience. Think of AI as a helpful assistant, not a replacement for your own judgment.

AI Resume Prompt

Prompt

You are a senior recruiter with 15+ years of experience in technical hiring and resume optimization. You have reviewed thousands of resumes for Clinical Research Coordinator positions and know exactly what hiring managers and ATS systems look for.

Your task:
Analyze my resume for a Clinical Research Coordinator position and provide concrete, actionable feedback to maximize my chances.

Job description:
[paste the job description here]

Provide feedback on the following:

  1. Match analysis: Which requirements from the job description ARE and ARE NOT reflected in my resume?
  2. Quantification: Which bullet points lack concrete numbers/metrics? Provide examples of how I can rewrite them.
  3. Keywords: Which technical terms from the job description (such as Microsoft Excel, Microsoft Office software, Microsoft PowerPoint, etc.) are missing or could be more prominent?
  4. Impact statements: Rewrite my 3 weakest bullet points using the STAR format (Situation, Task, Action, Result)
  5. ATS optimization: What adjustments will increase my score in Applicant Tracking Systems?
  6. Priorities: Give me a top-5 of changes that will make the biggest difference, ranked by impact.

Be direct and critical - I want honest feedback, not compliments.

Why use Mokaru instead? At Mokaru, we have invested extensive research into our AI prompts and continuously update them based on recruiter feedback and ATS testing. Our AI resume builder handles the complexity for you: optimizing for ATS systems, matching job descriptions, and ensuring professional formatting, so you can focus on landing interviews.

Clinical Research Coordinator Resume Example

Looking for a Clinical Research Coordinator resume instead? The skills and experience are very similar to a Clinical Research Coordinator. Here is an example you can use as inspiration:

OLIVIA THOMPSON

Clinical Research Coordinator
olivia.thompson@email.com • +1 (555) 123-4567 • San Francisco, CA

Summary

Clinical Research Coordinator with 8+ years of experience managing Phase II-IV oncology and cardiovascular trials. Streamlined participant enrollment for a multi-site study, accelerating recruitment by 30% against target. Proficient in full protocol lifecycle coordination, from screening to data collection, utilizing EDC systems and SPSS for analysis.

Skills

Technical: Microsoft Excel, Microsoft Office software, Microsoft PowerPoint, Microsoft Word, Microsoft Access, IBM SPSS Statistics
Professional: Reading Comprehension, Active Listening, Writing, Speaking, Coordination

Experience

Nexus Clinical Trials Management
2022 - Present
Lead Clinical Research Coordinator
  • Led protocol development and strategic planning for a multi-center Phase III trial, leveraging critical thinking and coordination to accelerate regulatory approval by 20%
  • Directed cross-functional team training on complex protocol procedures using Microsoft PowerPoint, improving team compliance and reducing protocol deviations by 15%
  • Implemented a comprehensive subject monitoring system using Microsoft Access, enhancing social perceptiveness in adverse event tracking and improving data quality by 25%
Apex Research Solutions Group
2019 - 2022
Clinical Research Coordinator II
  • Managed all aspects of patient scheduling and data collection for a 150-subject study, utilizing Microsoft Excel to coordinate appointments and maintain 98% protocol adherence
  • Authored and submitted all institutional review board documentation and progress reports, applying strong writing skills to secure timely approvals with zero major revisions
  • Performed statistical analysis of preliminary data using IBM SPSS Statistics, presenting findings that supported a key protocol amendment and improved subject retention
Veritas Clinical Management Partners
2016 - 2019
Associate Clinical Research Coordinator
  • Screened over 200 potential subjects through medical record reviews and interviews, applying active listening to accurately assess eligibility against strict protocol criteria
  • Prepared all study-related documentation and worksheets under senior supervision, utilizing Microsoft Word to ensure consistency and support regulatory audit readiness
  • Conducted patient interviews and performed protocol procedures like vital signs, applying reading comprehension to precisely execute tasks and maintain data integrity

Education

State University
2011 - 2015
Bachelor of Science

Certifications

  • Certified Clinical Research Professional (CCRP)
  • Project Management Professional (PMP)
  • Human Subjects Research (HSR) Certification

Build Your Clinical Research Coordinator Resume

Create a professional, ATS-optimized resume tailored for Clinical Research Coordinator positions in minutes.

Create Free Resume

Frequently Asked Questions

Ready to build your Clinical Research Coordinator resume?

Join thousands of professionals who have landed their dream job with Mokaru. Our AI-powered resume builder creates ATS-optimized resumes in minutes.

SSL Secured
GDPR Compliant
Secure Payments by Stripe
99.9% Uptime

© 2026 Mokaru. All rights reserved. Platform metrics based on user surveys, individual results may vary.