R&D, Farmacovigilanza & Affari Regolatori

Ricerca, sviluppo, test e lancio di nuove soluzioni farmacologiche. Il processo di sviluppo dura da 8 a 10 anni e si compone di 4 fasi.

R&D, Farmacovigilanza & Affari Regolatori
Ricerca, sviluppo, test e lancio di nuove soluzioni farmacologiche. Il processo di sviluppo dura da 8 a 10 anni e si compone di 4 fasi.

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Titolo	Luogo	Data	Req ID
Titolo	Luogo	Data (dd/MM/yy)	Req ID	Azzera
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
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
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
CMC Technical Leader CMC Technical Leader Europe - remote / US - remote, IT 4 nov 2025 6137	Europe - remote / US - remote, IT	4 nov 2025	6137
INTERN - Process Technologist INTERN - Process Technologist Parma, IT 4 nov 2025 6228	Parma, IT	4 nov 2025	6228
INTERN - Patient Engagement INTERN - Patient Engagement PARMA, IT 3 nov 2025 5993	PARMA, IT	3 nov 2025	5993
Clinical Trial Administrator - Maternity leave Clinical Trial Administrator - Maternity leave Flexible, IT 29 ott 2025 5768	Flexible, IT	29 ott 2025	5768
Sr. Manager, Regulatory Affairs Sr. Manager, Regulatory Affairs United States, US 29 ott 2025 6203	United States, US	29 ott 2025	6203
Sr. Director, Clinical Programs, Global Rare Diseases Sr. Director, Clinical Programs, Global Rare Diseases Boston, MA, US 29 ott 2025 6205	Boston, MA, US	29 ott 2025	6205
Sr. Manager, CMC Regulatory Affairs Sr. Manager, CMC Regulatory Affairs United States, US 27 ott 2025 6204	United States, US	27 ott 2025	6204
Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Ad Promo Manager, Americas Regulatory Affairs, Global Rare Diseases Boston, MA, US 26 ott 2025 6005	Boston, MA, US	26 ott 2025	6005
Preclinical Disease Area Expert Preclinical Disease Area Expert Parma, IT 25 ott 2025 4852	Parma, IT	25 ott 2025	4852
Clinical Program Lead Clinical Program Lead Cary, NC, US 25 ott 2025 5950	Cary, NC, US	25 ott 2025	5950
Senior Director, Global Patient Safety Science Senior Director, Global Patient Safety Science Everywhere in Europe, IT 24 ott 2025 6078	Everywhere in Europe, IT	24 ott 2025	6078
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 23 ott 2025 6111	Europe, IT	23 ott 2025	6111
Quality Manager Quality Manager Vienna, AT 23 ott 2025 6195	Vienna, AT	23 ott 2025	6195
Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Senior Clinical Research Physician Non-Obstructive Respiratory Diseases Parma, IT 21 ott 2025 5448	Parma, IT	21 ott 2025	5448
Global R&D QA, Senior GMP Product Compliance Specialist Global R&D QA, Senior GMP Product Compliance Specialist Parma, IT 21 ott 2025 6098	Parma, IT	21 ott 2025	6098
Sr. Director, R&D External Opportunities Sr. Director, R&D External Opportunities Parma, IT 19 ott 2025 5830	Parma, IT	19 ott 2025	5830
Translational and Precision Medicine Lead Translational and Precision Medicine Lead Europe - remote, GB 15 ott 2025 6152	Europe - remote, GB	15 ott 2025	6152

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