We are excited to announce an opportunity for a skilled and experienced Senior Regulatory Affairs Associate to join our dynamic and expanding team at Parexel. This role can be either home or office-based in Croatia, Romania, Poland, Lithuania, Czechia, and Hungary.
As a Senior Regulatory Affairs Associate, you will bring valuable experience in the field of Regulatory Affairs, particularly in Clinical Trial Applications (CTA) from various European locations. You will have the chance to work on regulatory submissions for Parexel as well as on projects dedicated to our clients.
If you are passionate about regulatory affairs and want to contribute to the success of our organization and clients, we invite you to apply for this exciting opportunity!
Parexel is offering a comprehensive benefits package to ensure your success and growth in this role. We provide training and knowledge of our organization’s basic consulting models, methodologies, as well as an understanding of the services we offer. Moreover, you will receive support from our senior staff to accomplish more complex tasks successfully.
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