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Clinical Study Manager (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Support
Projektbeschreibung
338533/11
IHRE AUFGABEN:
-Conduct clinical studies to support regulatory submissions
-Assist in the preparation of clinical study reports, regulatory documents and submissions
-Monitor and assist in monitoring activities to ensure compliance with study protocols, regulatory requirements and procedures
-Organise and lead internal and external meetings with associated communications and materials
IHRE QUALIFIKATIONEN:
-Bachelor degree in life sciences or related field
-CCRP or CCRA certification desired
-Experience in the medical device or pharmaceutical industry in a clinical research setting
-Experience with Clinical Trial Management systems, Trial Master File systems, and electronic data capture
-Advanced knowledge of industry standards and best practices in clinical data management and regulations (US FDA, ISO, ICH)
-Study/project management skills
-Fluency in English, German is of advantage
WEITERE QUALIFIKATIONEN:
Clinical project manager
Projektdetails
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Einsatzort:
Thedinghausen, Deutschland
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Projektbeginn:
asap
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Projektdauer:
3 MM++
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
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