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Consultancy in the area of Medical Writing
Eingestellt von FERCHAU GmbH aus Gummersbach
Projektbeschreibung
* Supervision and coordination of the preparation of documentation for regulatory submissions (investigator brochures, protocols, and clinical study reports) in technical coordination with other team members / CROs
* Timeline planning and participation at the project meetings as required
write strategic submission documents (IMPDs, briefing documents, clinical summaries)
VORAUSSETZUNGEN:
* Experience with clinical and non-clinical study report
* Experience in medical writing in the area of oncology
* Experience with regulatory submissions
* Experience with CROs
* Experience with local/regional studies, manuscripts, promotion writing, and clinical assumptions
* Fluency in written and spoken English
Projektdetails
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Einsatzort:
Darmstadt, Deutschland
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Projektbeginn:
asap
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Projektdauer:
41 Woche(n)
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges