2025. 12. 11. | Teljes munkaidõ | ParexelWith health authority requirements. The role can be home or office based in various European locations. Role Responsibilities Support global and/or local regulatory teams with comprehensive understanding of regional and global regulatory requirements Manage post-authorization lifecycle maintenance procedures
Nézze később2025. 12. 11. | Teljes munkaidõ | Budapest | ParexelWith health authority requirements. The role can be home or office based in various European locations. Role Responsibilities Support global and/or local regulatory teams with comprehensive understanding of regional and global regulatory requirements Manage post-authorization lifecycle maintenance procedures
Nézze később2025. 12. 11. | Teljes munkaidõ | ParexelManagement across multiple regions. The role can be home or office based in various European locations. Role Responsibilities Support Global Labelling, Regulatory (Clinical/Safety), or Medical Writing teams for labelling updates Manage Company Core Datasheet (CCDS) implementation into labelling and artworks
Nézze később2025. 12. 11. | Teljes munkaidõ | Budapest | ParexelManagement across multiple regions. The role can be home or office based in various European locations. Role Responsibilities Support Global Labelling, Regulatory (Clinical/Safety), or Medical Writing teams for labelling updates Manage Company Core Datasheet (CCDS) implementation into labelling and artworks
Nézze később2025. 12. 11. | Teljes munkaidõ | ParexelAnd Pharma top 50. And we have an incredible pipeline of work. Expect exciting professional challenges in inspiring studies, but with time for your outside life. This will be a fully remote home-based position. RAVE experience is strongly preferred. Responsibilities Lead a large clinical study or a series
Nézze később2025. 12. 10. | Teljes munkaidõ | Budapest | ParexelBe office or home based in various European locations. As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products. Primary Tasks
Nézze később2025. 12. 09. | Teljes munkaidõ | ParexelBe office or home based in various European locations. As the Regulatory Affairs Consultant you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products. Primary Tasks
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