Regulatory Affairs and Patient Safety Talent Pool (North and South America)
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Job Location:
New Brunswick, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
12 hours ago
Vacancies:
1 Vacancy
Job Summary
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds 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 were 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 Parexels commitment to delivering safe highquality care by identifying risks monitoring safety events andpromoting 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.
Key Skills
- Proofreading
- Adobe Acrobat
- FDA Regulations
- Manufacturing & Controls
- Biotechnology
- Clinical Trials
- Research & Development
- GLP
- cGMP
- Product Development
- Chemistry
- Writing Skills
About Company
Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our the ... View more
