F&E, Pharmakovigilanz & Regulatory Affairs

F&E, Pharmakovigilanz & Regulatory Affairs

Forschung, Entwicklung, Testung und Einführung neuer Arzneimittel. Der Entwicklungsprozess dauert 8 bis 10 Jahre und besteht aus 4 Phasen.

  • F&E, Pharmakovigilanz & Regulatory Affairs

    Forschung, Entwicklung, Testung und Einführung neuer Arzneimittel. Der Entwicklungsprozess dauert 8 bis 10 Jahre und besteht aus 4 Phasen.
Stellenbezeichnung Standort Datum Sort descending Req ID
Zurücksetzen
Clinical Trial Documentation & Records Management Lead
Clinical Trial Documentation & Records Management Lead Parma, IT 19.12.2025 6428
Parma, IT 19.12.2025 6428
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 18.12.2025 5448
Parma, IT 18.12.2025 5448
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026 Cary, NC, US 18.12.2025 6413
Cary, NC, US 18.12.2025 6413
Senior Director, Clinical Biometrics & Analytics
Senior Director, Clinical Biometrics & Analytics Parma, IT 16.12.2025 6387
Parma, IT 16.12.2025 6387
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 12.12.2025 6152
Europe - remote, GB 12.12.2025 6152
INTERN - Traslational Chemistry & Technology Innovation Lab Tech
INTERN - Traslational Chemistry & Technology Innovation Lab Tech Parma, IT 12.12.2025 6338
Parma, IT 12.12.2025 6338
Statistical Programmer
Statistical Programmer Europe - remote, FR 11.12.2025 6151
Europe - remote, FR 11.12.2025 6151
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 06.12.2025 5902
Europe - Remote, IT 06.12.2025 5902
EU Regulatory Affairs Manager, Rare Diseases
EU Regulatory Affairs Manager, Rare Diseases Parma, IT 05.12.2025 6145
Parma, IT 05.12.2025 6145
Global Project Lead
Global Project Lead United States, US 04.12.2025 6141
United States, US 04.12.2025 6141
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 03.12.2025 6228
Parma, IT 03.12.2025 6228
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 02.12.2025 5993
PARMA, IT 02.12.2025 5993
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US 27.11.2025 6203
United States, US 27.11.2025 6203
Sr. Director, Clinical Programs, Global Rare Diseases
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 27.11.2025 6205
Boston, MA, US 27.11.2025 6205
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Italy, Sweden, IT 26.11.2025 6307
Italy, Sweden, IT 26.11.2025 6307
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 25.11.2025 6204
United States, US 25.11.2025 6204
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 24.11.2025 6005
Boston, MA, US 24.11.2025 6005
Senior Analytical Scientist Biologics
Senior Analytical Scientist Biologics Parma, IT 24.11.2025 6192
Parma, IT 24.11.2025 6192
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT 22.11.2025 6078
Everywhere in Europe, IT 22.11.2025 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 21.11.2025 6111
Europe, IT 21.11.2025 6111