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.

Results 1 – 23 of 23 Page 1 of 1

Title	Location	Date	Req ID
Title	Location	Date (dd/MM/y)	Req ID	Reset
Translational and Precision Medicine Lead Translational and Precision Medicine Lead Europe - remote, GB 15 Oct 2025 6152	Europe - remote, GB	15 Oct 2025	6152
Sr. Director, R&D External Opportunities Sr. Director, R&D External Opportunities Parma, IT 19 Oct 2025 5830	Parma, IT	19 Oct 2025	5830
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 21 Oct 2025 5448	Parma, IT	21 Oct 2025	5448
Global R&D QA, Senior GMP Product Compliance Specialist Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT 21 Oct 2025 6098	Parma, IT	21 Oct 2025	6098
Quality Manager Quality Manager Vienna, AT 23 Oct 2025 6195	Vienna, AT	23 Oct 2025	6195
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 23 Oct 2025 6111	Europe, IT	23 Oct 2025	6111
Senior Director, Global Patient Safety Science Senior Director, Global Patient Safety Science Everywhere in Europe, IT 24 Oct 2025 6078	Everywhere in Europe, IT	24 Oct 2025	6078
Preclinical Disease Area Expert Preclinical Disease Area Expert Parma, IT 25 Oct 2025 4852	Parma, IT	25 Oct 2025	4852
Clinical Program Lead Clinical Program Lead Cary, NC, US 25 Oct 2025 5950	Cary, NC, US	25 Oct 2025	5950
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 26 Oct 2025 6005	Boston, MA, US	26 Oct 2025	6005
Sr. Manager, CMC Regulatory Affairs Sr. Manager, CMC Regulatory Affairs United States, US 27 Oct 2025 6204	United States, US	27 Oct 2025	6204
Sr. Manager, Regulatory Affairs Sr. Manager, Regulatory Affairs United States, US 29 Oct 2025 6203	United States, US	29 Oct 2025	6203
Sr. Director, Clinical Programs, Global Rare Diseases Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 29 Oct 2025 6205	Boston, MA, US	29 Oct 2025	6205
Clinical Trial Administrator - Maternity leave Clinical Trial Administrator - Maternity leave Flexible, IT 29 Oct 2025 5768	Flexible, IT	29 Oct 2025	5768
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
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
Global Project Lead Global Project Lead United States, US 5 Nov 2025 6141	United States, US	5 Nov 2025	6141
Statistical Programmer Statistical Programmer Europe - remote, FR 6 Nov 2025 6151	Europe - remote, FR	6 Nov 2025	6151
EU Regulatory Affairs Manager, Rare Diseases EU Regulatory Affairs Manager, Rare Diseases Parma, IT 6 Nov 2025 6145	Parma, IT	6 Nov 2025	6145
Medical Writing Manager Medical Writing Manager Parma, IT 7 Nov 2025 5903	Parma, IT	7 Nov 2025	5903
Clinical Program Leader Clinical Program Leader Europe - Remote, IT 7 Nov 2025 5902	Europe - Remote, IT	7 Nov 2025	5902

Results 1 – 23 of 23 Page 1 of 1