Medical Writer for clinical study protocols phase I and IIa, cardiovascular (m/f)

- home office  ‐ Remote
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Beschreibung


We are looking for a
Medical Writer for clinical study protocols phase I and IIa, cardiovascular (m/f)

Reference: -en
Start: asap
Duration: 6 MM
Place: - home office
Branch: Pharmazeutische Industrie

Your tasks:
  • Medical writing for clinical study protocols (cardiovascular)
  • Complete writing tasks satisfying all regulatory requirements and quality standards and meeting all project timelines
  • Review and carry out QC checks of all documents and appendices to ensure consistency between and within documents


Your qualifications
  • University degree in natural sciences etc.
  • Experience in the pharmaceutical industry in Medical Writing of clinical study protocols in Phase I + IIa
  • Profound knowledge in cardiovascular studies
  • Familiarity with clinical research, statistics, and regulatory guidance, standards and requirements regarding 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



Skills:
- Medical writer


Keywords: Medical Writer
Start
ab sofort
Dauer
6 MM
Von
Hays AG
Eingestellt
29.09.2015
Ansprechpartner:
Kerstin Werner
Projekt-ID:
990398
Vertragsart
Freiberuflich
Einsatzart
100 % Remote
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