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.
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.