F&E, Pharmakovigilanz & Regulatory Affairs

F&E, Pharmakovigilanz & Regulatory Affairs

Forschung, Entwicklung, Testung und Einführung neuer Arzneimittel. Der Entwicklungsprozess dauert 8 bis 10 Jahre und besteht aus 4 Phasen.

  • F&E, Pharmakovigilanz & Regulatory Affairs

    Forschung, Entwicklung, Testung und Einführung neuer Arzneimittel. Der Entwicklungsprozess dauert 8 bis 10 Jahre und besteht aus 4 Phasen.
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Stellenbezeichnung Standort Sort descending Datum Req ID
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Principal Medical Writer
Principal Medical Writer Toronto, Canada, CA 05.09.2024 4226
Toronto, Canada, CA 05.09.2024 4226
Academic Collaborations Management Intern
Academic Collaborations Management Intern Parma, IT 23.08.2024 4401
Parma, IT 23.08.2024 4401
Analytical Scientist
Analytical Scientist Parma, IT 17.08.2024 4299
Parma, IT 17.08.2024 4299
Medical Device, Combinations & Food Supplements Vigilance Lead
Medical Device, Combinations & Food Supplements Vigilance Lead Parma, IT 17.08.2024 4364
Parma, IT 17.08.2024 4364
Manufacturing & Technology Transfer Lab Tech Intern
Manufacturing & Technology Transfer Lab Tech Intern Parma, IT 07.09.2024 4480
Parma, IT 07.09.2024 4480
Specialist, Labelling & Compliance Regulatory Affairs, Global Rare Diseases
Specialist, Labelling & Compliance Regulatory Affairs, Global Rare Diseases Parma, IT 07.09.2024 4319
Parma, IT 07.09.2024 4319
In vivo pharmacology technician
In vivo pharmacology technician Parma, IT 21.08.2024 4508
Parma, IT 21.08.2024 4508
Senior Strategic Technical Leader
Senior Strategic Technical Leader Parma, IT 16.08.2024 4258
Parma, IT 16.08.2024 4258
Strategic Technical Leader
Strategic Technical Leader Parma, IT 16.08.2024 4258
Parma, IT 16.08.2024 4258
GCST and GPST Project Manager, Rare Diseases
GCST and GPST Project Manager, Rare Diseases Parma, IT 04.09.2024 4473
Parma, IT 04.09.2024 4473
Library and Information Specialist
Library and Information Specialist Parma, IT 14.08.2024 4273
Parma, IT 14.08.2024 4273
Clinical Project Manager
Clinical Project Manager Paris, Bois Colombes, FR 05.09.2024 3823
Paris, Bois Colombes, FR 05.09.2024 3823
Specialist Regulatory Affairs & Pharmacovigilance (all genders)
Specialist Regulatory Affairs & Pharmacovigilance (all genders) Hamburg, DE 05.09.2024 4469
Hamburg, DE 05.09.2024 4469
R&D Global Project Leader - Rare Diseases
R&D Global Project Leader - Rare Diseases Global - Remote, IT 18.08.2024 3402
Global - Remote, IT 18.08.2024 3402
Clinical Program Leader - Asthma
Clinical Program Leader - Asthma Europe/US, IT 16.08.2024 4013
Europe/US, IT 16.08.2024 4013
Senior Patient Engagement Partner
Senior Patient Engagement Partner Europe, IT 14.08.2024 4359
Europe, IT 14.08.2024 4359
GPV Standards & Training Specialist
GPV Standards & Training Specialist Europe, IT 29.08.2024 4388
Europe, IT 29.08.2024 4388
Global Pharmacovigilance QPPV Office Specialist - Temporary
Global Pharmacovigilance QPPV Office Specialist - Temporary Europe, IT 30.08.2024 4296
Europe, IT 30.08.2024 4296
Clinical Program Leader
Clinical Program Leader Cary, NC, US 23.08.2024 4029
Cary, NC, US 23.08.2024 4029
Global Regulatory Affairs Manager
Global Regulatory Affairs Manager Cary, NC, US 16.08.2024 3967
Cary, NC, US 16.08.2024 3967
Global RA Specialist
Global RA Specialist Cary, NC, US 30.08.2024 4293
Cary, NC, US 30.08.2024 4293
Ad Promo Manager, Americas Regulatory Affairs, Rare Diseases
Ad Promo Manager, Americas Regulatory Affairs, Rare Diseases Cary, NC, US 05.09.2024 4312
Cary, NC, US 05.09.2024 4312
Lead Data Manager
Lead Data Manager Cary, NC, US 16.08.2024 4324
Cary, NC, US 16.08.2024 4324
Lead Statistician
Lead Statistician Cary, NC, US 16.08.2024 4323
Cary, NC, US 16.08.2024 4323
Medical information & Pharmacovigilance Officer
Medical information & Pharmacovigilance Officer Brussels, BE 23.08.2024 3883
Brussels, BE 23.08.2024 3883