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DRA Project Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
REFERENZNUMMER:
274850/11
IHRE AUFGABEN:
-Acquire and maintain an overview of relevant regulatory requirements
-Creation and finalization of key regulatory documents (IMPD) as well as ensuring submission to HA (EU), scientific advice packages, Module 1 documents for EU and support for global submissions MAA
-Represent DRA in lifecycle, CT and other project-related meetings
IHRE QUALIFIKATIONEN:
-Bachelor degree in life sciences, medicine, pharmacy or equivalent
-Basic knowledge of regulatory legislation and guidelines
-Familiarity with clinical trial methodology
-Excellent English skills, both verbal and written
WEITERE QUALIFIKATIONEN:
Regulatory affairs assistant
274850/11
IHRE AUFGABEN:
-Acquire and maintain an overview of relevant regulatory requirements
-Creation and finalization of key regulatory documents (IMPD) as well as ensuring submission to HA (EU), scientific advice packages, Module 1 documents for EU and support for global submissions MAA
-Represent DRA in lifecycle, CT and other project-related meetings
IHRE QUALIFIKATIONEN:
-Bachelor degree in life sciences, medicine, pharmacy or equivalent
-Basic knowledge of regulatory legislation and guidelines
-Familiarity with clinical trial methodology
-Excellent English skills, both verbal and written
WEITERE QUALIFIKATIONEN:
Regulatory affairs assistant
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges