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.

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Translational and Precision Medicine Lead
Translational and Precision Medicine Lead Europe - remote, GB 12 Dec 2025 6152
Europe - remote, GB 12 Dec 2025 6152
Statistical Programmer
Statistical Programmer Europe - remote, FR 11 Dec 2025 6151
Europe - remote, FR 11 Dec 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 Clinical Project Manager
Senior Clinical Project Manager United States, US 2 Dec 2025 6275
United States, US 2 Dec 2025 6275
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 Dec 2025 6338
INTERN - Process Technologist
INTERN - Process Technologist Parma, IT 3 Dec 2025 6228
Parma, IT 3 Dec 2025 6228
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 2 Dec 2025 5993
PARMA, IT 2 Dec 2025 5993
Global Project Lead
Global Project Lead United States, US 4 Dec 2025 6141
United States, US 4 Dec 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 Dec 2025 6145
CMC Technical Leader
CMC Technical Leader Europe - remote / US - remote, IT 3 Dec 2025 6137
Europe - remote / US - remote, IT 3 Dec 2025 6137
Clinical Program Leader, R&D Global Rare Diseases
Clinical Program Leader, R&D Global Rare Diseases Europe - remote, GB 4 Dec 2025 6146
Europe - remote, GB 4 Dec 2025 6146
Clinical Program Leader
Clinical Program Leader Europe - Remote, IT 6 Dec 2025 5902
Europe - Remote, IT 6 Dec 2025 5902
Clinical Pharmacologist Lead
Clinical Pharmacologist Lead Parma, IT 26 Nov 2025 6307
Parma, IT 26 Nov 2025 6307
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 24 Nov 2025 6005