Clinical Research Project Manager Resume Example & Writing Guide
Use this Clinical Research Project Manager resume example and guide to improve your career and write a powerful resume that will separate you from the competition.
Clinical research is an expansive field that encompasses everything from designing and managing clinical trials to monitoring the safety of new drugs once they hit the market. Clinical research project managers oversee the research process from start to finish, ensuring that studies are conducted efficiently and effectively.
As a clinical research project manager, you’ll work closely with doctors, nurses, patients, and other healthcare professionals to ensure that studies are designed well, executed on time and on budget, and deliver accurate results. You’ll also coordinate with research sponsors (pharmaceutical companies, medical device manufacturers, etc.) to identify study goals and define success metrics. And you’ll oversee the collection and analysis of data once studies are complete.
Here are some tips and an example to help you write a fantastic clinical research project manager resume that will get you noticed by recruiters.
How to Write a Clinical Research Project Manager Resume
Here’s how to write a 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 explaining how you contributed to the organization.
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 timely recruitment of over 200 participants and no delays in trial completion on schedule.”
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 project manager role, your resume is likely to be scanned by an applicant tracking system (ATS) for certain keywords. This software looks for certain terms that are commonly used in clinical research, like “clinical trials” or “phase I.” If your resume doesn’t have enough of the right keywords, the ATS might discard your application.
To make sure your resume makes it past the ATS, focus on including relevant keywords throughout all sections of your resume. Here are some examples:
- Good Clinical Practice (GCP)
- Clinical Trials
- Clinical Research
- Clinical Development
- Clinical Monitoring
- Clinical Operations
- Electronic Data Capture (EDC)
- CRO Management
- Clinical Trial Management System (CTMS)
- Protocol
- Standard Operating Procedure (SOP)
- Clinical Development Planning
- Regulatory Submissions
- Clinical Data Management
- Protocol Development
- Clinical Trial Monitoring
- Clinical Trial Assurance
- Life Sciences
- Oncology
- Therapeutic Areas
- Clinical Research Management
- Regulatory Affairs
- Clinical Trial Implementation
- Oncology Clinical Research
- CMC Regulatory Requirements
- Good Clinical Practice Regulations
- Pharmacovigilance
- Protocol Assessment
- Informed Consent
- Institutional Review Board (IRB)
Showcase Your Technical Skills
As a clinical research project manager, you will be responsible for overseeing and coordinating clinical trials. 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 recruitment databases. You will also need to have a solid understanding of the regulatory landscape and be familiar with the guidelines set forth by the FDA.