Clinical Research Coordinator Resume Writing Tips and Sample

Looking for a new CRC role? Your clinical research coordinator resume needs to clearly communicate your skills and experience to help you land a job interview. This document is often the first thing a hiring manager or principal investigator sees, so take the time to improve it before you begin applying for CRC jobs.

Clinical research coordinator and research nurse resumes need to highlight more than patient care. Hiring teams are looking for candidates who understand study protocols, regulatory requirements, and data integrity, while still using a patient-centered approach. Use the following tips as you write or update your resume for clinical research coordinator positions:

• Keep it focused and readable: Prioritize research-related duties and outcomes over lengthy job descriptions. Clarity matters more than design or flashy layouts.
• Highlight research-specific skills: Include experience with informed consent, institutional review board submissions, regulatory compliance, data collection, and study coordination tools.
• Tailor your resume summary or objective: Use keywords from the job posting to show how your background aligns with the specific study population or therapeutic area.
• Translate clinical experience: If you’re coming from bedside nursing, you can still emphasize clinical research coordinator resume skills like patient education, documentation accuracy, and care coordination.
• Include certifications and training: List any training, certifications, research coursework, or continuing education related to clinical trials.

Looking for more support? Use our clinical research coordinator resume sample to help you confidently move from application to interview.

Sample Resume for Clinical Research Coordinator

Casey Datafield, RN BSN

City, State
email@email.com / (555) 123-4567
linkedin.com/caseydatafield

Experienced clinical research coordinator with 5+ years of experience managing Phase I–III clinical trials across academic and industry-sponsored studies. Strong background in patient recruitment, regulatory compliance, and study coordination, with a proven ability to ensure adherence to ICH-GCP guidelines and FDA regulations.

Professional Experience

Clinical Research Coordinator II, Academic Medical Center (June 20XX – Present)

• Coordinate daily operations for 5+ active Phase II and III clinical trials across oncology and internal medicine.
• Screen and enroll eligible patients, conduct informed consent discussions, and educate participants on study protocols.
• Ensure compliance with ICH-GCP guidelines, FDA regulations, and institutional SOPs.
• Assess, document, and report adverse events and serious adverse events to the PI and sponsors.
• Prepare and maintain regulatory binders, institutional review board submissions, protocol amendments, and continuing reviews.
• Serve as primary liaison between sponsors, monitors, investigators, and study teams.
• Support study budgeting, billing reconciliation, and financial tracking.
• Participate in sponsor monitoring visits and internal audits with zero major findings.

Clinical Research Coordinator I, Community Hospital Research Institute (August 20XX – May 20XX)

• Assisted with coordination of industry-sponsored cardiology and endocrinology trials.
• Recruited and followed study participants, scheduled visits, and coordinated labs and procedures.
• Collected and entered study data into electronic data capture systems.
• Maintained accurate source documentation and case report forms.
• Supported regulatory submissions and ensured timely reporting to IRB and sponsors.
• Collaborated with nursing staff and providers to integrate research protocols into clinical workflows.

Registered Nurse I, medical-surgical, Academic Medical Center (June 20XX – July 20XX)

• Provided direct patient care to a diverse adult population in an inpatient setting.
• Developed strong assessment, documentation, and patient education skills.
• Collaborated with interdisciplinary teams to deliver safe, evidence-based care.

Core Skills

• Patient screening and informed consent
• Adverse event (AE/SAE) reporting
• Institutional review board submissions and regulatory binders
• Study start-up and close-out
• Sponsor and monitor communication
• Budget tracking and study billing
• Electronic data capture systems
• Source documentation and data integrity

Education

Bachelor of Science in Nursing, State University

Licensure & Certifications

Registered Nurse (RN), License #123456
Certified Clinical Research Professional (CCRP)
Basic Life Support (BLS)

Professional Affiliations

Association of Clinical Research Professionals (ACRP)
Society of Clinical Research Associates (SOCRA)

Clinical Research Coordinator Salary

On average, a CRC’s salary is about $53,660 per year, but this varies widely by location, experience, certifications, and responsibilities. If you’re interested in relocating, consider opportunities in the highest-paying states for RNs:

• California
• Hawaii
• Oregon
• Washington
• Massachusetts

Put Your Clinical Research Coordinator Resume to Work

IntelyCare has opportunities for clinical research coordinators, nursing professionals, and more. If you’re in the market for a new job, check out our nursing job board to learn more.