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 Sort descending Ubicación Fecha Req ID
Restablecer
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 12 dic 2025 6152
Europe - remote, GB 12 dic 2025 6152
Statistical Programmer
Statistical Programmer Europe - remote, FR 11 dic 2025 6151
Europe - remote, FR 11 dic 2025 6151
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
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT 22 nov 2025 6078
Everywhere in Europe, IT 22 nov 2025 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 21 nov 2025 6111
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 19 nov 2025 5448
Senior Analytical Scientist Biologics
Senior Analytical Scientist Biologics Parma, IT 24 nov 2025 6192
Parma, IT 24 nov 2025 6192
INTERN - Traslational Chemistry & Technology Innovation Lab Tech Parma, IT 12 dic 2025 6338
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 3 dic 2025 6228
Parma, IT 3 dic 2025 6228
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 2 dic 2025 5993
PARMA, IT 2 dic 2025 5993
Global Project Lead
Global Project Lead United States, US 4 dic 2025 6141
United States, US 4 dic 2025 6141
Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT 19 nov 2025 6098
EU Regulatory Affairs Manager, Rare Diseases Parma, IT 5 dic 2025 6145
Clinical Program Leader, R&D Global Rare Diseases
Clinical Program Leader, R&D Global Rare Diseases Europe - remote, GB 4 dic 2025 6146
Europe - remote, GB 4 dic 2025 6146
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 6 dic 2025 5902
Europe - Remote, IT 6 dic 2025 5902
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Italy, Sweden, IT 26 nov 2025 6307
Italy, Sweden, IT 26 nov 2025 6307
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 24 nov 2025 6005