Clinical Research Coordinator

Writing a great clinical research coordinator resume is important because it is one of the first things a potential employer will see when they are considering you for a position. It is your opportunity to make a good first impression and sell yourself as the best candidate for the job.

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If you're looking for inspiration when it comes to drafting your own clinical research coordinator resume, look no further than the samples below. These resumes will help you highlight your experience and qualifications in the most effective way possible, giving you the best chance of landing the clinical research coordinator job you're after.

Resume samples

Camren Rugnetta | (431) 534-4222 | Yukon, OK


I am a Clinical Research Coordinator with over 3 years of experience. I have coordinated numerous clinical trials from start to finish and have gained unparalleled knowledge in the field. I possess excellent organizational skills, which has allowed me to manage multiple projects simultaneously while maintaining attention to detail. My interpersonal skills are superb, allowing me to build strong relationships with Investigators, Vendors, and Sponsors alike. Furthermore, my oral and written communication abilities are top-notch; thus ensuring that all study documentation is accurate and compliant


Clinical Research Coordinator at St. Jude Children's Research Hospital, OKApr 2022 - Present

  • Led clinical research team of 5 in conducting studies with over 500 participants.
  • Wrote and submitted 3 successful grant applications, resulting in $1.5 million in funding.
  • Successfully recruited hard-to-reach patient populations for clinical trials.
  • Managed budget and vendors for all aspects of clinical research projects.
  • Monitors patients progress during trial to ensure safety according to study protocol.
  • Served as primary liaison between sponsor companies and investigative sites.

Clinical Research Associate at Mayo Clinic, OKJul 2019 - Mar 2022

  • Led clinical research studies with up to 50 participants, ensuring all procedures were followed and data was collected accurately.
  • Monitored patients during study periods to ensure their safety and well-being.
  • Wrote detailed reports of findings for each study.
  • Trained new Clinical Research Associates on company policies and procedures.
  • Reviewed medical charts and histories to identify potential candidates for upcoming studies.
  • Presented results of completed studies at scientific conferences.


Bachelor of Science in Clinical Research at Oklahoma State University, OKAug 2014 - May 2019

I've learned how to develop research proposals, how to manage research projects, and how to communicate research findings.


  • Good communication skills
  • Organizational skills
  • Detail oriented
  • Ability to work independently
  • Strong computer skills
  • Knowledge of medical terminology
  • Clinical research experience

Zadie Marchioli | (783) 108-4357 | 6893 Blue Spruce Drive


I am a Clinical Research Coordinator with over 3 years of experience. I have coordinated and managed clinical trials from start to finish, ensuring that all aspects of the trial are carried out according to protocol. I have also been responsible for training and supervising research staff, as well as maintaining accurate records and documenting any adverse events that occur during the course of a study. My strong organizational skills and attention to detail ensure that all trials are conducted smoothly and efficiently, while my excellent communication skills enable me to effectively liaise with sponsors, monitors, patients and other members of the research team.


Clinical Research Coordinator at Rocky Mountain Research Laboratory, MTJun 2022 - Present

  • Led clinical study for new cancer drug with 80 patients, which resulted in the FDA approving the drug for public use.
  • Worked on a team of 5 people to develop a new clinical research protocol that was adopted by 3 different hospitals.
  • Trained 4 new Clinical Research Coordinators on proper documentation and patient care procedures.
  • Was responsible for data entry and analysis for a 12-month long heart disease study with 300 participants.
  • Successfully completed IATA Dangerous Goods Shipping certification.
  • CPR/BLS certified.

Clinical Research Associate at Northwest Clinical Trials, MTAug 2019 - May 2022

  • Led the clinical research for a new drug that was approved by the FDA, resulting in $100 million in annual sales.
  • Managed a team of 10 Clinical Research Associates and helped train them on Good Clinical Practices.
  • Wrote 5 SOPs (Standard Operating Procedures) that are now used company-wide.
  • Researched and published 3 papers in peer-reviewed journals.
  • Negotiated with 6 different Institutional Review Boards to get approval for our studies.
  • Monitors compliance with GCP/ICH guidelines.


Bachelor of Science in Clinical Research at Montana State University, Bozeman, MTAug 2014 - May 2019

I have learned how to conduct clinical research studies, how to work with patients, and how to analyze data.


  • Clinical research
  • Regulatory affairs
  • Clinical operations
  • Project management
  • Data management
  • Budgeting and finance
  • Contract negotiation