R&D, Pharmacovigilance & Regulatory Affairs_uk

R&D, Pharmacovilance & Regulatory Affairs

Researching, developing, testing and launching new drug solutions. The development process lasts from 8 to 10 years and is made up of 4 phases.

  • R&D, Pharmacovilance & Regulatory Affairs

    Researching, developing, testing and launching new drug solutions. The development process lasts from 8 to 10 years and is made up of 4 phases.

Title Location Date Sort ascending Req ID
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INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 3 Nov 2025 5993
PARMA, IT 3 Nov 2025 5993
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 4 Nov 2025 6228
Parma, IT 4 Nov 2025 6228
CMC Technical Leader
CMC Technical Leader Europe - remote / US - remote, IT 4 Nov 2025 6137
Europe - remote / US - remote, IT 4 Nov 2025 6137
Global Project Lead
Global Project Lead United States, US 5 Nov 2025 6141
United States, US 5 Nov 2025 6141
Clinical Program Leader, R&D Global Rare Diseases
Clinical Program Leader, R&D Global Rare Diseases Europe - remote, GB 5 Nov 2025 6146
Europe - remote, GB 5 Nov 2025 6146
EU Regulatory Affairs Manager, Rare Diseases Parma, IT 6 Nov 2025 6145
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 7 Nov 2025 5902
Europe - Remote, IT 7 Nov 2025 5902
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 13 Nov 2025 6152
Europe - remote, GB 13 Nov 2025 6152
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 19 Nov 2025 5448
Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT 19 Nov 2025 6098
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 21 Nov 2025 6111
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 Analytical Scientist Biologics
Senior Analytical Scientist Biologics Parma, IT 24 Nov 2025 6192
Parma, IT 24 Nov 2025 6192
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 24 Nov 2025 6005
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 25 Nov 2025 6204
United States, US 25 Nov 2025 6204
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Parma, IT 26 Nov 2025 6307
Parma, IT 26 Nov 2025 6307
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 27 Nov 2025 6205
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US 27 Nov 2025 6203
United States, US 27 Nov 2025 6203