Clinical Research Monitor Resume Example & Writing Guide

Use this Clinical Research Monitor resume example and guide to improve your career and write a powerful resume that will separate you from the competition.

Clinical research monitors oversee clinical trials, making sure they run smoothly and safely. They monitor the progress of research projects, ensuring that they follow protocol and meet regulatory requirements. They monitor clinical studies to ensure that they follow ethical guidelines and that patients are protected. And they monitor the safety of the treatments being tested by making sure that study participants are free from adverse reactions.

If you enjoy helping people and want to be part of something bigger than yourself, clinical research monitoring might be the perfect job for you. Here are some tips and an example resume to help you write a compelling clinical research monitor resume that will get you noticed by recruiters.

James Smith
Los Angeles, CA | (123) 456-7891 | [email protected]

Highly experienced clinical research monitor with a passion for protecting the safety and welfare of human subjects. Over eight years of experience in the pharmaceutical industry, specializing in Phase I-III trials. Skilled in clinical trial monitoring, data management, and GCP compliance.

University of California, Irvine Jun '10
B.S. in Biological Sciences
Company A, Clinical Research Monitor Jan '17 – Current
  • Monitored clinical trials for safety and adherence to protocol, providing regular reports to the Principal Investigator (PI) and Clinical Research Associate (CRA).
  • Assisted with recruitment of patients into studies by contacting potential participants over the phone or in person.
  • Provided support to investigators during study procedures such as phlebotomy, EKG monitoring, etc., ensuring that all required documentation is completed accurately and on time.
  • Maintained accurate records of patient visits including dates, times, diagnoses/problems, treatments provided, medications prescribed/administered, tests performed and results obtained.
  • Performed other duties as assigned by management such as assisting with preparation of documents related to regulatory submissions or preparing data for analysis by a statistician.
Company B, Clinical Research Monitor Jan '12 – Dec '16
  • Assisted in the development of a new clinical trial for an FDA-approved drug, which led to increased patient enrollment and improved study efficiency
  • Conducted weekly site visits to monitor research staff performance, ensuring that all procedures were being followed correctly
  • Supervised data collection and analysis activities as well as overall project management throughout the duration of each study
  • Collaborated with medical personnel on issues related to protocol compliance, adverse events and safety concerns
  • Provided training on monitoring techniques and regulatory requirements for junior Clinical Research Monitors
Company C, Clinical Research Coordinator Jan '09 – Dec '11
  • Managed projects through various stages of the project lifecycle (e.g., initiation, execution, close-out).
  • Provided project/data support including study start-up activities such as protocol and regulatory document management; vendor contracting and negotiation; budgeting; equipment procurement, maintenance, and disposal; space planning and development to ensure adequate resources for research needs by working with other departments within the hospital.
  • Supervised clinical research associates involved in all aspects of clinical trials from recruitment through completion & submission of final reporting requirements.
  • Certified Clinical Research Coordinator
  • Clinical Research Associate
  • Clinical Research Manager

Industry Knowledge: HIPAA, IRB, Clinical Trial Management System, Electronic Case Report Form
Technical Skills: Case Report Form, CRF, HIPAA, IRB, ECRF, SAS, SPSS, Microsoft Office Suite
Soft Skills: Critical Thinking, Problem Solving, Good Judgment, Teamwork, Communication, Attention to Detail

How to Write a Clinical Research Monitor Resume

Here’s how to write a clinical research monitor resume of your own.

Write Compelling Bullet Points

Bullet points are the most effective way to showcase your experience and qualifications. But rather than simply listing your responsibilities, you can make your bullet points much more interesting and compelling by using specific numbers and metrics.

For example, rather than saying you “conducted research on new drug candidates,” you could say you “conducted research on new drug candidates, resulting in a 15% increase in candidate selection rate.”

The second bullet point is much more specific and provides a clear indication of the outcome of your work. And that’s what hiring managers want to see—evidence of your ability to get results.

Identify and Include Relevant Keywords

When you apply for a clinical research monitor job, your resume is likely to go through an applicant tracking system (ATS). This software scans your resume for certain keywords related to the position. If your resume doesn’t have enough of the right keywords, the ATS might filter out your application.

One way to make sure your resume makes it past the ATS is to include relevant keywords throughout all the sections. You can find a list of common clinical research monitor keywords below:

  • Good Clinical Practice (GCP)
  • Clinical Trials
  • Clinical Research
  • Clinical Monitoring
  • Clinical Development
  • Standard Operating Procedure (SOP)
  • CRO Management
  • Protocol
  • Regulatory Submissions
  • Biotechnology
  • Oncology
  • Clinical Operations
  • Regulatory Affairs
  • Biomedical Research
  • Medical Education
  • Life Sciences
  • CRMC
  • Clinical Data Management
  • Informatics
  • Clinical Safety
  • Data Monitoring
  • Electronic Data Capture (EDC)
  • Clinical Trial Management System (CTMS)
  • Standard Protocol
  • Patient Safety
  • Oncology Research
  • SAEs
  • Good Clinical Practice Regulations
  • Ethics
  • Data Analysis

Showcase Your Technical Skills

As a clinical research monitor, you will be responsible for overseeing clinical trials and ensuring that they are conducted according to protocol. This will require you to be proficient in the use of various software programs and systems, such as electronic data capture (EDC) systems, clinical trial management systems (CTMS), and patient portals. You will also need to be able to use Microsoft Office Suite programs, such as Word, Excel, and PowerPoint, to create reports and presentations.


Economic Development Specialist Resume Example & Writing Guide

Back to Resume

Talent Acquisition Partner Resume Example & Writing Guide