Regulatory Affairs Specialist

5 dni temu


Warszawa, Mazovia, Polska TN Poland Pełny etat

Indero, a contract research organization specialized in dermatology and rheumatology, is seeking a highly skilled Regulatory Affairs Specialist. As a key member of our team, you will be responsible for ensuring the quality and compliance of regulatory documents and submissions. This role requires strong knowledge of EU regional regulatory guidelines and excellent organizational skills.

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The ideal candidate will have at least 2 years of experience in regulatory affairs, with expertise in preparing and submitting part I and/or part II Clinical trial applications following EU CTR. They will also possess excellent leadership skills, as they will provide guidance on all regulatory activities leading to the start-up of clinical trials. Additionally, they will work collaboratively within an expansion mode environment.


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This role is perfect for individuals who are passionate about regulatory affairs and have a strong desire to share their knowledge of applicable EU regional regulatory guidelines. If you thrive in a collaborative environment and are committed to delivering high-quality results, we encourage you to apply.



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