Nada Alkis
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Personal Information
Organização/Local de trabalho
Copenhagen Area, Capital Region, Denmark Denmark
Cargo
Pharmacist / Regulatory Affairs / Clinical Trials
Setor
Medical / Health Care / Pharmaceuticals
Site
www.linkedin.com/in/nadaalkis/
Sobre
A highly structured, motivated, and responsible certified pharmacist. Additionally, graduate with master in Pharmaceutical Science from University of Copenhagen specialized in clinical trials and regulatory affairs. Offering year and half hands-on experience working at Novo Nordisk. I am looking to develop my skills within clinical trials and regulatory affairs even further.
Detalhes do contato
Marcadores
chronic obstructive pulmonary disease human immunodeficiency virus hypertension type-2 diabetes asthma label therapeutic indication substitution add-on initial combination data analysis regulatory affairs master thesis patient-reported outcomes real-world evidence clinical trial regulations medicine research regulatory
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Apresentações

(1)

Nada Alkis' Master Thesis Presentation 16.01.2018

Há 5 anos • 304 Visualizações

Documentos

(1)

Nada Alkis' Master Thesis, Novo Nordisk & University of Copenhagen

Há 5 anos • 430 Visualizações
Personal Information
Organização/Local de trabalho
Copenhagen Area, Capital Region, Denmark Denmark
Cargo
Pharmacist / Regulatory Affairs / Clinical Trials
Setor
Medical / Health Care / Pharmaceuticals
Site
www.linkedin.com/in/nadaalkis/
Sobre
A highly structured, motivated, and responsible certified pharmacist. Additionally, graduate with master in Pharmaceutical Science from University of Copenhagen specialized in clinical trials and regulatory affairs. Offering year and half hands-on experience working at Novo Nordisk. I am looking to develop my skills within clinical trials and regulatory affairs even further.
Marcadores
chronic obstructive pulmonary disease human immunodeficiency virus hypertension type-2 diabetes asthma label therapeutic indication substitution add-on initial combination data analysis regulatory affairs master thesis patient-reported outcomes real-world evidence clinical trial regulations medicine research regulatory
Ver mais