Regulatory Affairs and Patient Safety Talent Pool (North and South America)
This a Full Remote job, the offer is available from: South America, United States, Brazil, Argentina, Mexico, Canada
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Explore Your Next Chapter in Regulatory Affairs or Patient Safety
At Parexel, we value the expertise and dedication of regulatory and patient safety 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 and Patient Safety 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.
Patient Safety roles support Parexel's commitment to delivering safe, high‑quality care by identifying risks, monitoring safety events, and promoting continuous process improvement.
• Patient Safety Associate - supporting the review, documentation, and tracking of patient safety events and assisting in analyzing trends and risks
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.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
This offer from "Parexel" has been enriched by Jobgether.com and got a 87% flex score.
Apply Now
Apply Now
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Explore Your Next Chapter in Regulatory Affairs or Patient Safety
At Parexel, we value the expertise and dedication of regulatory and patient safety 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 and Patient Safety 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.
Patient Safety roles support Parexel's commitment to delivering safe, high‑quality care by identifying risks, monitoring safety events, and promoting continuous process improvement.
• Patient Safety Associate - supporting the review, documentation, and tracking of patient safety events and assisting in analyzing trends and risks
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.
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
This offer from "Parexel" has been enriched by Jobgether.com and got a 87% flex score.
Apply Now
Apply Now