Regulatory Affairs Talent Pool (EMEA & Australia)
Parexel
This listing was originally posted on Parexel's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
Upgrade to Pro to access the AI-generated 'Read before applying' briefing and other premium pharma intelligence.
Upgrade to Pro — $25/moWhen 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!
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!
Explore related positions you might be interested in
We'll notify you when matching roles are posted.
Interviewed at Parexel?
Help others prepare — share your experience anonymously.
CRO
Upgrade to Pro to access AI interview prep brief and other premium pharma intelligence.
Upgrade to Pro — $25/moUpgrade to Pro to access salary benchmarks and market rate data and other premium pharma intelligence.
Upgrade to Pro — $25/mo