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
R&D Manufacturing & Technology Transfer Manager Parma, IT 20 ene 2026 6501
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT 19 ene 2026 6078
Everywhere in Europe, IT 19 ene 2026 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 18 ene 2026 6111
Clinical Trial Documentation & Records Management Lead Parma, IT 17 ene 2026 6428
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026 Cary, NC, US 16 ene 2026 6413
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases UK, GB 16 ene 2026 5448
Senior Director, Clinical Biometrics & Analytics Parma, IT 14 ene 2026 6387
INTERN - Traslational Chemistry & Technology Innovation Lab Tech Parma, IT 10 ene 2026 6338
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 10 ene 2026 6152
Europe - remote, GB 10 ene 2026 6152
Statistical Programmer
Statistical Programmer Europe - remote, FR 9 ene 2026 6151
Europe - remote, FR 9 ene 2026 6151
Pharmazeut (all genders) im Praktikum für 2026 / 2027 Hamburg, DE 8 ene 2026 351
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 4 ene 2026 5902
Europe - Remote, IT 4 ene 2026 5902
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 1 ene 2026 6228
Parma, IT 1 ene 2026 6228
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 31 dic 2025 5993
PARMA, IT 31 dic 2025 5993
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 26 dic 2025 6205
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US 26 dic 2025 6203
United States, US 26 dic 2025 6203
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Italy, Sweden, IT 25 dic 2025 6307
Italy, Sweden, IT 25 dic 2025 6307
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 24 dic 2025 6204
United States, US 24 dic 2025 6204