06.09.2022 aktualisiert
CS
100 % verfügbar
Medical Writer
Waldshut-Tiengen, Deutschland
Deutschland
PhDSkills
Medical WriterScientific WritingMedical WritingClinical Study ProtocolClinical Study ReportRegulatory DocumentsInvestigator`s BrochureClinical Studyabstractmanuscript
In my >13 years of medical writing in small and big Pharma I have gained expertise
- in the preparation of
- regulatory and clinical documents (e.g. clinical study reports and protocols, briefing documents, investigator brochures, clinical summary documents) and
- medical communication materials (e.g., manuscripts, abstracts, oral and poster presentations)
- early clinical development (including first-in-human)
- vaccines, biosimilars, and diverse therapeutic areas (e.g., infectious diseases, oncology, neurodegenerative diseases)
- working efficiently with cross-functional project teams
Sprachen
DeutschMutterspracheEnglischgutFranzösischgutSpanischgutTürkischgut
Projekthistorie
Pharmacology projects
Associate Director Global Regulatory Medical Writing * Mentored, trained, and coordinated
internal and external Medical Writers
Associate Director Global Regulatory Medical Writing * Mentored, trained, and coordinated
internal and external Medical Writers
* Wrote or led the writing of clinical, regulatory, and safety documents both for early phase and
marketed products (infectious diseases)
* Registered clinical studies and posted results at public databases (clinicaltrials.gov)
marketed products (infectious diseases)
* Registered clinical studies and posted results at public databases (clinicaltrials.gov)