R&D, Pharmacovigilance & Regulatory Affairs

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.
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Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Parma, IT Nov 26, 2025 6307
Parma, IT Nov 26, 2025 6307
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US Nov 25, 2025 6204
United States, US Nov 25, 2025 6204
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US Nov 24, 2025 6005
Boston, MA, US Nov 24, 2025 6005
Analytical Bio Project Principal Scientist
Analytical Bio Project Principal Scientist Parma, IT Nov 24, 2025 6192
Parma, IT Nov 24, 2025 6192
Senior Director, Global Patient Safety Science
Senior Director, Global Patient Safety Science Everywhere in Europe, IT Nov 22, 2025 6078
Everywhere in Europe, IT Nov 22, 2025 6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT Nov 21, 2025 6111
Europe, IT Nov 21, 2025 6111
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT Nov 19, 2025 5448
Parma, IT Nov 19, 2025 5448
Global R&D QA, Senior GMP Product Compliance Specialist
Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT Nov 19, 2025 6098
Parma, IT Nov 19, 2025 6098
Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB Nov 13, 2025 6152
Europe - remote, GB Nov 13, 2025 6152
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT Nov 7, 2025 5902
Europe - Remote, IT Nov 7, 2025 5902
EU Regulatory Affairs Manager, Rare Diseases
EU Regulatory Affairs Manager, Rare Diseases Parma, IT Nov 6, 2025 6145
Parma, IT Nov 6, 2025 6145
Global Project Lead
Global Project Lead United States, US Nov 5, 2025 6141
United States, US Nov 5, 2025 6141
Clinical Program Leader, R&D Global Rare Diseases
Clinical Program Leader, R&D Global Rare Diseases Europe - remote, GB Nov 5, 2025 6146
Europe - remote, GB Nov 5, 2025 6146
CMC Technical Leader
CMC Technical Leader Europe - remote / US - remote, IT Nov 4, 2025 6137
Europe - remote / US - remote, IT Nov 4, 2025 6137
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT Nov 4, 2025 6228
Parma, IT Nov 4, 2025 6228
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT Nov 3, 2025 5993
PARMA, IT Nov 3, 2025 5993
Clinical Trial Administrator - Maternity leave
Clinical Trial Administrator - Maternity leave Flexible, IT Oct 29, 2025 5768
Flexible, IT Oct 29, 2025 5768
Sr. Manager, Regulatory Affairs
Sr. Manager, Regulatory Affairs United States, US Oct 29, 2025 6203
United States, US Oct 29, 2025 6203
Sr. Director, Clinical Programs, Global Rare Diseases
Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US Oct 29, 2025 6205
Boston, MA, US Oct 29, 2025 6205