Regulatory Affairs Consultant - Medical Devices Lead for Clinical Trials (home or office based)
When our values align, there's no limit to what we can achieve.
About the Role
We are seeking an experienced Regulatory Affairs professional to lead our medical devices and combination products clinical trial regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and serve as the key regulatory representative for our global project teams.
The role can be office or home based in various European locations.
Key Responsibilities
- functional teams to ensure timely and compliant regulatory submissions.
Skills and Experience required for the role:
- device combination products.
GMP.
Wise would be a plus.
- Informații detaliate despre oferta de muncă
Firma: Parexel Localiția: Bucureşti
Bucureşti Sectorul 1, București, RomaniaAdăugat: 29. 11. 2025
Postul de muncă activ
Fii primul, care se va înregistra la oferta de muncă respectivă!