Espoo, Finland and 2 more (Hybrid)
Orion Pharma’s Research and Development is looking for a Regulatory Affairs Specialist to support EU and global regulatory activities for our oncology and pain development‑stage pharmaceutical programs.
In this role, you will work under the guidance of senior regulatory professionals to prepare and manage regulatory submissions and contribute to cross‑functional project teams within R&D. This is an excellent opportunity for a junior‑to‑mid level regulatory professional to deepen hands‑on experience in clinical development and regulatory submissions. You will be part of a global team with colleagues based in the United States, United Kingdom, and Finland.