Oncology Regulatory Affairs Specialist: Submissions & Strategy

Orion Pharma’s Research and Development team seeks a Regulatory Affairs Specialist to support EU and global regulatory activities. This role involves preparing regulatory submissions and collaborating with cross-functional teams, providing hands-on experience in clinical development.

The ideal candidate should have a Bachelor’s or Master’s degree and 2+ years of regulatory affairs experience, with strong communication skills and a quality-driven mindset. The position offers competitive compensation and a collaborative culture.

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