Beschreibung
* Overseeing and coordinating the preparation of documentation for regulatory submissions (e.g., investigator brochures, protocols, and clinical study reports) in collaboration with other team members or CROs* Writing strategic submission documents (e.g., IMPDs, briefing documents, clinical summaries) with the aim to ensure the quality of documents
* Master or Ph.D. in the scientific area (Oncology)
* Experience in Medical Writing in the area of Oncology (min. 2-3 years)
* Experience with regulatory submissions
* Experience with CROs
* Experience with clinical and non-clinical studies
* Experience with local/regional studies, manuscripts, promotion writing, clinical assumptions
* English: Business fluent, German: nice to have
Remote (for minimum 30 h/week, including training in Darmstadt for ca. 1 week)
Schlagwörter:
Medical Writing, Medizinische Dokumentation, Clinial trial, Oncology, Onkologie, Arzt, Mediziner, Pharmazeut, Pharmazie, Pharmacy, Krebs, Biology, Biologie, Chemie, Chemistry, Cancer, Freelance, Freelancer, Freiberuflich, freiberufler, Darmstadt
Kontaktperson: Personalreferentin Frau Julia-Elisabeth Kratz
FERCHAU GmbH
Niederlassung Darmstadt
Rösslerstr. 88
64293 Darmstadt