Jobs at Parexel
Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Regulatory Affairs Talent Pool (EMEA & Australia)
Job ID R0000037388 , United KingdomExplore 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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