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Medical Writer for Clinical Study Protocols Phase I and IIa, Oncology (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
284217/8
IHRE AUFGABEN:
-Medical writing for clinical study protocols (oncology)
-Complete writing tasks satisfying all regulatory requirements and quality standards and meeting all project timelines
-Review and execute QC checks of all documents and appendices to ensure consistency
IHRE QUALIFIKATIONEN:
-University degree in Medicine or Pharmacy
-Experience in the pharmaceutical industry in Medical Writing of clinical study protocols in Phase I + IIa
-Profound knowledge in oncology
-Familiarity with clinical research, statistics, and regulatory guidance, standards and requirements pertaining to regulatory medical writing world-wide (e.g. ICH, FDA, EMEA)
-Experience in electronic document management
-Strong English communication skills, in both written and verbal form
WEITERE QUALIFIKATIONEN:
Medical writer
Projektdetails
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Einsatzort:
Home-Office, Deutschland
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Projektbeginn:
asap
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Projektdauer:
6 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