I contribute to clinical research with expertise and empathy. And I do it
Regulatory Affairs Talent Pool (US & Canada)
Primary Location: United States, Remote Additional Locations: Canada, Ontario, Remote Job ID R0000037394 Category Regulatory Affairs Date Posted 12/16/2025Overview
As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Problem-solver
- Relationship-builder
- Results-driven
- Strategic
About This Role
Explore Your Next Chapter in Regulatory Affairs
At Parexel, we value the expertise and dedication of regulatory professionals who are passionate about advancing global health. This career page highlights opportunities where your skills can make a meaningful impact in shaping the future of drug development.
We also recognize the importance of flexibility in how you work. Our Regulatory Affairs opportunities offer the ability to work remotely from home, empowering you to contribute globally while maintaining balance in your personal and professional life.
Regulatory Affairs is a diverse and dynamic field, offering pathways for specialists across multiple disciplines:
• Labeling Operations – ensuring accuracy and compliance in product information.
• Labeling Strategy – shaping global labeling approaches to meet evolving regulatory requirements.
• Advertising & Promotion – guiding compliant communications that balance innovation with patient safety.
• Chemistry, Manufacturing, and Controls (CMC) – driving product quality and development through technical and regulatory expertise.
• Regional and Global Health Authority Expertise – leveraging direct experience with agencies worldwide to navigate complex approval processes.
• Regulatory Operations & Publishing – managing submission processes, document publishing, and ensuring timely delivery of compliant dossiers.
If you are interested in learning more, we invite you to express your interest in joining Parexel. Explore the opportunities available and discover how your expertise can help us deliver solutions that improve patients’ lives worldwide.
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EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Employee Insights
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