Clinical Research Manager Resume Example & Writing Guide
Use this Clinical Research Manager resume example and guide to improve your career and write a powerful resume that will separate you from the competition.
Clinical research managers oversee clinical trials and are responsible for managing research staff, overseeing study design and implementation, and ensuring that research projects are completed on time and within budget.
If you enjoy working with numbers and science but have ambitions that extend beyond your current role, becoming a clinical research manager could be a fantastic next step in your career. Here are some tips for writing a compelling clinical research manager resume plus an example for reference.
How to Write a Clinical Research Manager Resume
Here’s how to write a clinical research manager resume of your own.
Write Compelling Bullet Points
When you’re writing bullet points, it can be tempting to simply list your responsibilities. But that’s not enough to make a strong impression. Instead, you should use your bullet points to demonstrate your value by highlighting your accomplishments, results, and contributions.
For example, rather than saying you “managed clinical trials for new drug development,” you could say that you “managed clinical trials for new drug development, resulting in 100% recruitment rate for Phase 1 trials and on-time completion of all studies.”
The second bullet point paints a much clearer picture of what you did and the results of your work. And that’s what hiring managers want to see!
Identify and Include Relevant Keywords
When you apply for a clinical research manager role, your resume will likely be scanned by an applicant tracking system (ATS) for certain keywords. This program will search your resume for terms related to the job, like “clinical trials” or “patient recruitment.” If your resume doesn’t have enough of the right keywords, the ATS might reject your application.
To make sure your resume makes it past the ATS, use this list of common clinical research manager keywords as a starting point:
- Clinical Research
- Good Clinical Practice (GCP)
- Clinical Development
- Clinical Monitoring
- Clinical Pharmacology
- Protocol
- CRO Management
- Clinical Trial Management System (CTMS)
- Standard Operating Procedure (SOP)
- Oncology
- Clinical Data Management
- Clinical Trials
- Biotechnology
- U.S. Food and Drug Administration (FDA)
- Clinical Research Management
- Regulatory Affairs
- Biomedical Research
- Validation
- Institutional Review Board (IRB)
- Molecular Biology
- Cell Culture
- Life Sciences
- Medicine
- Patient Safety
- Informatics
- Electronic Data Capture (EDC)
- Healthcare
- Good Clinical Practice Regulations
- Standard Operating Procedure Development
- Oncology Clinical Research
Showcase Your Technical Skills
As a clinical research manager, you need to be proficient in a variety of software programs and systems in order to do your job. Programs like Microsoft Office Suite, Excel, and PowerPoint are essential for managing and tracking clinical research data. Additionally, clinical research managers need to be familiar with the various types of software used in clinical research, such as electronic data capture (EDC) software and clinical trial management systems (CTMS). So if you have experience with any of these programs or systems, be sure to list them on your resume.