As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.
In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.
- Full Time
- Level: Mid
- Travel: Yes
- Glassdoor Reviews and Company Rating
Success Profile
Check out the top traits we're looking for and see if you have the right mix.
- Detail-Oriented
- Proactive
- Problem-Solver
- Results-Driven
- Organized
- Multi-Tasker
Rewards
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Collaboration
Work with industry leaders and subject matter experts.
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Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
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Variety
Opportunities to work on multiple accounts – never boring!
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Management
Strong management with depth of experience working for global health authorities.
Responsibilities
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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