Description
Medical Writer for regulatory documents (m/f)
Reference: -en
Start: 02/19
Duration: 12 MM
Main tasks:
- Accountable for 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
- Write strategic submission documents (e.g. IMPDs, briefing documents, clinical summaries)
Main qualifications
- In-depth Medical Writing experience
- Solid knowledge and experience with writing protocols, clinical summaries, clinical study reports
- Demonstrated solid project management skills
- Fluency in English (verbal and written) and German (verbal and written)
- Experience with multi tasking
- Attention to detail/strong organizational skills
Main advantages:
- Fulltime project
- Renowned company
About us:
With over 15 years of experience in the pharmaceutical industry, biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated professionals looking to develop themselves professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – all completely free of charge. Register with us and reap the benefits of job offers that are both interesting and relevant to your skills and experience.
My contact at Hays:
My contact person:
Tatiana Hahl
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