Clinical Research Nurse

Writing a great clinical research nurse 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 nurse 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 nurse job you're after.

Resume samples

Zuleica Garoner

zuleica.garoner@gmail.com | (102) 694-1531 | Charleston, SC

Summary


I am a Clinical Research Nurse with over 3 years of experience. I have worked on a variety of research studies, including clinical trials and observational studies. I have also served as a liaison between the research team and the patients/participants. In this role, I provided support to patients throughout their participation in the study, answered any questions they had, and helped to ensure that their rights were protected. Additionally, I assisted with data collection and analysis for the study.

Experience


Clinical Research Nurse Manager at Roper St. Francis Healthcare, SCJun 2022 - Present

  • Led a team of 12 clinical research nurses in conducting over 100 clinical trials.
  • Coordinated with principal investigators and sponsors to ensure that all trials were conducted according to protocol.
  • Monitored patient progress throughout each trial and reported any adverse events immediately.
  • Trained new staff on proper procedures for conducting clinical trials.
  • Wrote monthly reports summarizing the status of ongoing trials.

Clinical Research Nurse at MUSC Health, SCSep 2019 - Apr 2022

  • Led a team of 5 nurses in conducting clinical research for a new cancer treatment.
  • Recruited 100 patients for the clinical trial.
  • Monitored patient progress and reported data to the research team.
  • Assisted in developing protocols for future trials.
  • Presented findings at national conferences.

Education


Bachelor of Science in Nursing at University of South CarolinaSep 2015 - May 2019

Some skills I've learned are critical thinking, time management, communication, and teamwork.

Skills


  • Nursing
  • Clinical research
  • Patient care
  • Communication
  • Documentation
  • Organizational skills
  • Time management

Myrtice Ferrall

myrtice.ferrall@gmail.com | (348) 028-8444 | 504 W Main St, Fairfield, IA 52556, United States

Summary


I am a Clinical Research Nurse with over 3 years of experience working in clinical research settings. I have a strong background in patient care and nursing, as well as experience coordinating and conducting clinical trials. I am detail-oriented and organized, with excellent communication skills. I am passionate about providing high-quality patient care and contributing to the advancement of medical research.

Experience


Clinical Research Nurse Manager at MercyOne, IAApr 2022 - Present

  • Led a team of 10 clinical research nurses and coordinators in conducting over 30 Phase I-III clinical trials.
  • Managed budgets totaling $2M annually for all departmental operations and personnel.
  • Developed standard operating procedures (SOPs) for the conduct of clinical trials which are now being used company-wide.
  • Chaired or co-chaired 4 Institutional Review Board (IRB) committees responsible for reviewing human subjects research protocols.
  • Successfully recruited 150 patients to participate in studies across a broad range of therapeutic areas including oncology, cardiology, pulmonology, etc.
  • Monitors were very satisfied with 97% site visits.

Clinical Research Nurse at UnityPoint Health, IASep 2019 - Mar 2022

  • Led clinical research trials for new medications, treatments and procedures with a 97% success rate.
  • Recruited an average of 15 patients per month to participate in clinical research trials.
  • Monitored patient progress throughout the duration of the trial and reported any adverse effects to the principal investigator.
  • Collaborated with physicians, pharmacists and other healthcare professionals to ensure that all aspects of the trial were conducted according to protocol.
  • Managed budget for assigned projects ensuring efficient use of resources while maintaining quality standards.

Education


Bachelor of Science in Nursing at Iowa State University, Ames, IAAug 2015 - May 2019

I have learned how to communicate effectively with patients and families, how to work as part of a team, and how to provide high-quality nursing care.

Skills


  • Nursing
  • Clinical research
  • Patient care
  • Data collection
  • Medical chart review
  • IRB submissions
  • Regulatory compliance