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 descending Req ID
Restablecer
Head of Clinical Project Management
Head of Clinical Project Management Italy, IT 21 ago 2026 7386
Italy, IT 21 ago 2026 7386
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 20 ago 2026 5993
PARMA, IT 20 ago 2026 5993
Clinical Research Physician, Global Rare Diseases
Clinical Research Physician, Global Rare Diseases Europe - Remote, IT 20 ago 2026 7356
Europe - Remote, IT 20 ago 2026 7356
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Cary, NC, US 20 ago 2026 7551
R&D Process Excellence & Digital Solutions Senior Manager Parma, IT 17 ago 2026 7313
Senior Global Patient Safety Physician
Senior Global Patient Safety Physician Europe, remote, IT 15 ago 2026 7401
Europe, remote, IT 15 ago 2026 7401
R&D Data Visualization Engineer
R&D Data Visualization Engineer Parma, IT 15 ago 2026 7301
Parma, IT 15 ago 2026 7301
Clinical Operations Lead
Clinical Operations Lead Italy remote, IT 15 ago 2026 7376
Italy remote, IT 15 ago 2026 7376
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Parma, IT 15 ago 2026 7394