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Drug Regulatory Affairs Project Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
- Global Regulatory Affairs in development of products (Phases II-III)
- Creating the briefing book for health authorities
- IMPD (Investigational Medicinal Product Dossier) for the CTAs (Clinical Trial Applications)
- Work with indications of Psoriasis and MS
- Profound experience in Drug Regulatory Affair (development)
- Experience in working with health authorities EMA/EU and FDA
- Ability to creat briefing books for health authorities
- Deep knowledge of Investigational Medicinal Product Dossier and Clinical Trial Application
- Very good English skills
Weitere Qualifikationen: Regulatory affairs manager
- Creating the briefing book for health authorities
- IMPD (Investigational Medicinal Product Dossier) for the CTAs (Clinical Trial Applications)
- Work with indications of Psoriasis and MS
- Profound experience in Drug Regulatory Affair (development)
- Experience in working with health authorities EMA/EU and FDA
- Ability to creat briefing books for health authorities
- Deep knowledge of Investigational Medicinal Product Dossier and Clinical Trial Application
- Very good English skills
Weitere Qualifikationen: Regulatory affairs manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges
Hays
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Straße:
Willy-Brandt-Platz 1-3
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Ort:
68161 Mannheim, Universitätsstadt, Deutschland