Clinical Data Coordinator

Writing a great clinical data 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 data 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 data coordinator job you're after.

Resume samples

Brya Beighley | (164) 965-7592 | 267 A Street,


I am a Clinical Data Coordinator with over 3 years of experience. I have worked in both small and large clinical settings, and have experience coordinating data for all types of studies. I am highly organized and detail-oriented, and have a strong passion for helping others. I believe that my skills and experiences would make me an excellent addition to your team.


Clinical Data Coordinator at Clinical Data Coordinators, Inc., MAApr 2022 - Present

  • Led a team of 4 data coordinators in the clinical research department and successfully completed 12 studies within 6 months.
  • Ensured accuracy and timely delivery of study documents by conducting daily reviews and audits.
  • Trained new staff on clinical research processes and documentation requirements.
  • Maintained up-to-date knowledge of federal regulations governing clinical trials.
  • Streamlined data collection process, resulting in a 30% increase in efficiency.
  • Negotiated with insurance companies to obtain coverage for participants enrolled in clinical trials.

Clinical Data Coordinator II at The Clinical Data Coordination Group, LLC, MAJul 2019 - Mar 2022

  • Led the clinical data management for 4 studies with 20 sites and 300 subjects.
  • Reviewed, cleaned and verified the accuracy of study data entered into the EDC system by site staff.
  • Monitored site performance against Data Management Plan timelines and deliverables; identified issues/risks and recommended solutions to Project Manager.
  • Authored 6 Study Dataset Specifications according to CDISC standards.
  • Developed 8 edit check programs in ValidateIT per protocol requirements.
  • Generated 7 clean datasets meeting analysis specifications for biostatisticians.


Associate's Degree in Health Information Management at Bunker Hill Community College, MAAug 2015 - May 2019

Through my Associate's Degree in Health Information Management I have learned how to effectively manage and communicate health information.


  • Clinical Data Management
  • CDISC Standards
  • SAS Programming
  • SQL Database Management
  • EDC Systems (e.g., Medidata Rave, Oracle Clinical)
  • IWRS/IVRS Systems (e.g., Informa, Inc.)
  • Microsoft Office

Suzi Glisch | (125) 591-0040 | Grand Island, NE


I have over 3 years of experience working as a Clinical Data Coordinator. In this role, I was responsible for coordinating and managing clinical data for research studies. I also worked closely with the research team to ensure that all data was collected accurately and in compliance with study protocol. My experience has taught me how to effectively manage large amounts of data while ensuring accuracy and quality control.


Clinical Data Coordinator at CSC, NEJun 2022 - Present

  • Led a team of 4 clinical data coordinators in the successful completion of 3 clinical studies with over 1,000 participants.
  • Trained new staff on study protocols and data entry procedures.
  • Developed and implemented new quality control procedures that reduced errors by 50%.
  • Created customized reports for sponsors that provided detailed analysis of participant data.
  • Presented findings at national conferences on 2 occasions.
  • Authored 5 peer-reviewed journal articles related to clinical research methods and outcomes.

Clinical Data Coordinator II at CDM Smith, NEAug 2019 - Apr 2022

  • Led a team of 4 data coordinators in the abstraction and analysis of clinical data for 50 patients with chronic disease X.
  • Successfully completed the abstraction and analysis of clinical data for 100 patients with acute disease Y within 2 weeks.
  • Trained 3 new employees on proper data collection techniques and software use.
  • Created a new system for tracking patient information that increased efficiency by 30%.
  • Authored 5 SOPs related to Data Management processes that are now being used company-wide.
  • Presented findings from abstracted data at national conference, resulting in positive feedback from peers.


Associate's Degree in Health Information Management at Bellevue University, NEAug 2015 - May 2019

I have learned how to code medical diagnoses and procedures, as well as how to manage medical records.


  • Microsoft Office
  • Clinical Data Management Systems
  • SAS Programming
  • CDISC Standards
  • 21 CFR Part 11 Compliance
  • Good Clinical Practices (GCP)