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 Datum Sort descending Req ID
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Global Project Manager
Global Project Manager Cary, NC, US 17.04.2024 4012
Cary, NC, US 17.04.2024 4012
Senior DP Analytical Scientist
Senior DP Analytical Scientist Parma, IT 16.04.2024 3834
Parma, IT 16.04.2024 3834
Area Clinical Operations Lead
Area Clinical Operations Lead Parma, IT 15.04.2024 4004
Parma, IT 15.04.2024 4004
Clinical Project Manager
Clinical Project Manager Paris, Bois Colombes, FR 13.04.2024 3823
Paris, Bois Colombes, FR 13.04.2024 3823
eTMF Specialist
eTMF Specialist Boston, MA, US 13.04.2024 3557
Boston, MA, US 13.04.2024 3557
Global Project Manager
Global Project Manager Stockholm, IT 12.04.2024 3490
Stockholm, IT 12.04.2024 3490
Pharmacovigilance Specialist
Pharmacovigilance Specialist Parma, IT 11.04.2024 3596
Parma, IT 11.04.2024 3596
Clinical Project Manager
Clinical Project Manager Cary, NC, US 11.04.2024 3806
Cary, NC, US 11.04.2024 3806
Lead Clinical Research Associate
Lead Clinical Research Associate UK/France, IT 11.04.2024 3504
UK/France, IT 11.04.2024 3504
Global RA Labeling Unit Head
Global RA Labeling Unit Head Cary, NC, US 10.04.2024 3978
Cary, NC, US 10.04.2024 3978
Drug Substance Analytical Lead
Drug Substance Analytical Lead Parma or anywhere in Europe, IT 05.04.2024 2942
Parma or anywhere in Europe, IT 05.04.2024 2942
Regulatory Affairs Trainee
Regulatory Affairs Trainee Barcelona, ES 05.04.2024 3783
Barcelona, ES 05.04.2024 3783
Real World Evidence Study Manager - Temporary
Real World Evidence Study Manager - Temporary Parma, IT 04.04.2024 3946
Parma, IT 04.04.2024 3946
PV/QA & Specialist
PV/QA & Specialist Bratislava, SK 03.04.2024 3936
Bratislava, SK 03.04.2024 3936
Regulatory Affairs Specialist, Rare Diseases
Regulatory Affairs Specialist, Rare Diseases Cary, NC, US 01.04.2024 3928
Cary, NC, US 01.04.2024 3928
Rare Disease Clinical Project Manager
Rare Disease Clinical Project Manager Parma, IT 29.03.2024 3809
Parma, IT 29.03.2024 3809
Assoc Director, Advertising and Promotion, Commercial Labeling Lead, Americas Reg Affairs, GRD
Assoc Director, Advertising and Promotion, Commercial Labeling Lead, Americas Reg Affairs, GRD Cary, NC, US 28.03.2024 3804
Cary, NC, US 28.03.2024 3804
Clinical Research Physician
Clinical Research Physician Europe - remote, IT 27.03.2024 3609
Europe - remote, IT 27.03.2024 3609
R&D Global Project Leader - Rare Diseases
R&D Global Project Leader - Rare Diseases Global - Remote, IT 26.03.2024 3402
Global - Remote, IT 26.03.2024 3402
Rare Disease Clinical Research Physician
Rare Disease Clinical Research Physician Europe - remote, IT 26.03.2024 3507
Europe - remote, IT 26.03.2024 3507
Pharmaceutical Affairs Officer
Pharmaceutical Affairs Officer Brussels, BE 20.03.2024 3883
Brussels, BE 20.03.2024 3883
Global Regulatory Project Specialist
Global Regulatory Project Specialist Cary, NC, US 20.03.2024 3810
Cary, NC, US 20.03.2024 3810
Global Regulatory Project Specialist
Global Regulatory Project Specialist Cary, NC, US 20.03.2024 3810
Cary, NC, US 20.03.2024 3810