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 Req ID Sort ascending
Restablecer
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 18 dic 2025 5448
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 6 dic 2025 5902
Europe - Remote, IT 6 dic 2025 5902
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 2 dic 2025 5993
PARMA, IT 2 dic 2025 5993
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 24 nov 2025 6005
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT 21 dic 2025 6078
Everywhere in Europe, IT 21 dic 2025 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 20 dic 2025 6111
Global Project Lead
Global Project Lead United States, US 4 dic 2025 6141
United States, US 4 dic 2025 6141
EU Regulatory Affairs Manager, Rare Diseases Parma, IT 5 dic 2025 6145
Statistical Programmer
Statistical Programmer Europe - remote, FR 11 dic 2025 6151
Europe - remote, FR 11 dic 2025 6151
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 12 dic 2025 6152
Europe - remote, GB 12 dic 2025 6152
Senior Analytical Scientist Biologics
Senior Analytical Scientist Biologics Parma, IT 24 nov 2025 6192
Parma, IT 24 nov 2025 6192
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US 27 nov 2025 6203
United States, US 27 nov 2025 6203
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 25 nov 2025 6204
United States, US 25 nov 2025 6204
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 27 nov 2025 6205
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 3 dic 2025 6228
Parma, IT 3 dic 2025 6228
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Italy, Sweden, IT 26 nov 2025 6307
Italy, Sweden, IT 26 nov 2025 6307
INTERN - Traslational Chemistry & Technology Innovation Lab Tech Parma, IT 12 dic 2025 6338
Senior Director, Clinical Biometrics & Analytics Parma, IT 16 dic 2025 6387
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026 Cary, NC, US 18 dic 2025 6413
Clinical Trial Documentation & Records Management Lead Parma, IT 19 dic 2025 6428