Description
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