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Medical Writer
il y a 4 semaines
**Responsibilities**
Writing documents relating to the laboratory’s clinical development
- Search for information and documents to integrate into clinical study reports
- Writing scientific publications (posters, abstracts, articles, protocols, analysis plans, final reports)
- Writing and formatting of all clinical study report documents, consistent with the statistical report
- Participation in the drafting of supporting documents for the clinical study (use protocol, investigator and patient brochure, consent form, observation notebook and patient notebook, etc.)
- Anonymization in the context of documents submitted to the various health authorities in order to remove any confidential information (personal data & commercial data)
**key skills**
- Be comfortable and effective in communication, while being diplomatic
- Know how to work in a team and across departments (R&D, medical affairs, regulatory affairs, quality, legal, marketing and finance, subsidiaries/parent company)
- Have writing skills and a capacity for analysis and synthesis
- Be rigorous, autonomous and dynamic
- Have a keen sense of listening and communication
- Be flexible, adaptable and flexible
- Have ethics (respect for the patient and the confidentiality of this data)
- Have operational and fluent English
