Senior Regulatory Affairs Manager - Global Clinical Trial Services - Hybrid Opportunity
Are you ready to advance your career and join a business that is a leader in Clinical Services? This role provides the opportunity to specialize in a niche area of a business with three key divisions, offering exposure to an area of the pharmaceutical industry that is directly involved in saving the lives of some of the most vulnerable patients in the world.
As part of our close-knit regulatory team of three, you'll dive into developing intelligence materials, creating regulatory plans, and offering project-based support. You'll need a solid grasp of EU directives, US CFR, and GMP/GDP regulations.
Why this role?
* Delve into a classic RA position with a fantastic team of specialists.
* Opportunities to progress and learn new things in a fast-paced environment.
* This business's passion trumps any other, truly matching your work ethic in an extremely patient-focused space.
* One of the biggest service providers in this specialist area.
* Freedom to shape key parts of the regulatory team and function.
This is a unique opportunity to experience a wide range of responsibilities in a fast-paced industry. If you're passionate about clinical services and ready to contribute to a growing company, apply now and be a part of something big!
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