Join Parexel's Regulatory Affairs Team: Shape the Future of Healthcare
Parexel, a leading Clinical Research Organization, is seeking talented professionals at all levels to join our dynamic Regulatory Affairs and Operations team. We are looking for Associates, Consultants, and Senior Experts who are passionate about ensuring regulatory success in the ever-evolving pharmaceutical and biotechnology landscape.
Who We Are:At Parexel, our Regulatory Affairs team is at the forefront of global healthcare innovation. We work closely with health authorities worldwide, including the US-FDA, EMA, and NMPA, to develop unique regulatory strategies, secure submission approvals, and maintain compliance for trials and products across diverse therapeutic areas.
What We Offer:
Exposure to cutting-edge projects in Orphan Drug, Rare Disease, OTC Drug, Cell and Gene Therapies (C>), and more
Opportunity to work with global teams and clients
Career growth across various levels from Associate to Senior Consultant
Continuous learning and development in a rapidly evolving field
Possibility to work from home
Key Responsibilities Across Levels:
Ensure regulatory submissions and activities adhere to global health authority guidelines
Develop and execute regulatory strategies
Collaborate with cross-functional teams to drive project success
Maintain client relationships and deliver high-quality consultancy services
Stay updated on regulatory trends and contribute to process improvements
Requirements:
University-level education in Life Sciences
Previous experience in regulatory affairs (level-dependent)
Strong team spirit, flexibility, accountability, and organizational skills
Fluency in English (written and spoken)
Desire to grow in a fast-paced, innovative environment
Register your interest at Parexel and be part of a team that's shaping the future of healthcare through regulatory excellence. Whether you are starting your career or bringing years of expertise, we hope we can find a place for you to thrive and make a difference.
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