R&D, Pharmacovigilance & Regulatory Affairs_tr

Ar-Ge, Farmakovijilans ve Ruhsatlandırma İşleri

Yeni ilaç çözümleri araştırma, geliştirme, test etme ve piyasaya sürme. Geliştirme süreci 8 ila 10 yıl sürer ve 4 fazdan oluşur.

  • Ar-Ge, Farmakovijilans ve Ruhsatlandırma İşleri

    Yeni ilaç çözümleri araştırma, geliştirme, test etme ve piyasaya sürme. Geliştirme süreci 8 ila 10 yıl sürer ve 4 fazdan oluşur.

Arama terimi "". Sayfa 1/2, 1 ile 25 arasındaki sonuçlar - 29
Başlık Konum Tarih Sort ascending Req ID
Sıfırla
PV/QA & Specialist
PV/QA & Specialist Bratislava, SK 29 Haz 2024 3936
Bratislava, SK 29 Haz 2024 3936
Real World Evidence Study Manager - Temporary Parma, IT 30 Haz 2024 3946
Drug Substance Analytical Lead
Drug Substance Analytical Lead Parma or anywhere in Europe, IT 1 Tem 2024 2942
Parma or anywhere in Europe, IT 1 Tem 2024 2942
Global RA Specialist
Global RA Specialist Cary, NC, US 3 Tem 2024 4293
Cary, NC, US 3 Tem 2024 4293
GPV PSMF & Compliance Sr Specialist
GPV PSMF & Compliance Sr Specialist Parma, IT 3 Tem 2024 4283
Parma, IT 3 Tem 2024 4283
Global Reg-CMC Specialist
Global Reg-CMC Specialist Cary, NC, US 3 Tem 2024 4194
Cary, NC, US 3 Tem 2024 4194
Pharm Tech Technician - Temporary
Pharm Tech Technician - Temporary Parma, IT 5 Tem 2024 4175
Parma, IT 5 Tem 2024 4175
Clinical Project Manager
Clinical Project Manager Cary, NC, US 7 Tem 2024 3806
Cary, NC, US 7 Tem 2024 3806
Global Project Leader
Global Project Leader Boston, MA, US 9 Tem 2024 4310
Boston, MA, US 9 Tem 2024 4310
Ad Promo Manager, Americas Regulatory Affairs, Rare Diseases Cary, NC, US 9 Tem 2024 4312
Clinical Pharmacologist
Clinical Pharmacologist Europe remote, IT 9 Tem 2024 4313
Europe remote, IT 9 Tem 2024 4313
Clinical Project Manager
Clinical Project Manager Paris, Bois Colombes, FR 9 Tem 2024 3823
Paris, Bois Colombes, FR 9 Tem 2024 3823
eTMF Specialist
eTMF Specialist Boston, MA, US 9 Tem 2024 3557
Boston, MA, US 9 Tem 2024 3557
Principal Medical Writer
Principal Medical Writer Toronto, Canada, CA 9 Tem 2024 4226
Toronto, Canada, CA 9 Tem 2024 4226
Specialist, Labelling & Compliance Regulatory Affairs, Global Rare Diseases Parma, IT 11 Tem 2024 4319
Global Reg-CMC Sr. Specialist
Global Reg-CMC Sr. Specialist Parma, IT 12 Tem 2024 4235
Parma, IT 12 Tem 2024 4235
Global Regulatory Lead
Global Regulatory Lead Parma, IT 15 Tem 2024 4278
Parma, IT 15 Tem 2024 4278
Senior Patient Engagement Partner
Senior Patient Engagement Partner Europe, IT 16 Tem 2024 4359
Europe, IT 16 Tem 2024 4359
Project Statistician
Project Statistician Cary, NC, US 18 Tem 2024 4323
Cary, NC, US 18 Tem 2024 4323
Lead Data Manager
Lead Data Manager Cary, NC, US 18 Tem 2024 4324
Cary, NC, US 18 Tem 2024 4324
Global Regulatory Affairs Manager
Global Regulatory Affairs Manager Cary, NC, US 18 Tem 2024 3967
Cary, NC, US 18 Tem 2024 3967
Clinical Program Leader - Asthma
Clinical Program Leader - Asthma Europe/US, IT 18 Tem 2024 4013
Europe/US, IT 18 Tem 2024 4013
Senior Strategic Technical Leader
Senior Strategic Technical Leader Parma, IT 18 Tem 2024 4258
Parma, IT 18 Tem 2024 4258
Strategic Technical Leader
Strategic Technical Leader Parma, IT 18 Tem 2024 4258
Parma, IT 18 Tem 2024 4258
Analytical Scientist
Analytical Scientist Parma, IT 19 Tem 2024 4299
Parma, IT 19 Tem 2024 4299