I+D, farmacovigilancia y asuntos reglamentarios

I+D, Farmacovigilancia y Regulatory Affairs

Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.

  • I+D, Farmacovigilancia y Regulatory Affairs

    Investigar, desarrollar, probar y lanzar nuevas soluciones farmacológicas. El proceso de desarrollo dura de 8 a 10 años y consta de 4 fases.
Título Ubicación Fecha Sort ascending Req ID
Restablecer
Statistical Programmer
Statistical Programmer Parma, IT 4 sept 2026 7444
Parma, IT 4 sept 2026 7444
Principal Regulatory Writer, Global Rare Diseases
Principal Regulatory Writer, Global Rare Diseases Parma, IT 6 sept 2026 7341
Parma, IT 6 sept 2026 7341
R&D Bioinformatician Lead
R&D Bioinformatician Lead Parma, IT 6 sept 2026 7280
Parma, IT 6 sept 2026 7280
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 7 sept 2026 6111
Europe, IT 7 sept 2026 6111
Senior Technical Leader, Protein Biologics Development, GRD CMC
Senior Technical Leader, Protein Biologics Development, GRD CMC Parma, IT 10 sept 2026 7605
Parma, IT 10 sept 2026 7605
Senior Technical Leader, GRD CMC
Senior Technical Leader, GRD CMC Parma, IT 10 sept 2026 7607
Parma, IT 10 sept 2026 7607
Clinical Innovation Project Manager
Clinical Innovation Project Manager Italy, IT 10 sept 2026 7388
Italy, IT 10 sept 2026 7388
Senior Technical Leader, Analytical Method Development and Validation, GRD CMC
Senior Technical Leader, Analytical Method Development and Validation, GRD CMC Parma, IT 10 sept 2026 7606
Parma, IT 10 sept 2026 7606
PV/RA Manager
PV/RA Manager Zaventem, BE 11 sept 2026 7643
Zaventem, BE 11 sept 2026 7643