My client is an innovating, dynamic and growing international medical device company currently expanding their clinical team in Switzerland, Geneve Canton.
Due to this growth my client is looking for a Medical / Scientific Writer.
The position will report to the Head of Clinical Development Department.
Your Responsabilities :
Prepares and finalises clinical documents such as, but not limited to, CSRs and appendices, IBs, protocols and protocol amendments, summary documents, RMPs (initial and updates), regulatory responses, and briefing documents.
Leads cross-functional document planning and review meetings
Responsible for functional planning and metrics database updates for assigned program.
Ihr Profil :
PhD or Master in elated Pharmaceutical Science with minimum 3 years experience of relevant regulatory medical writing
Strong project management skills
Strong leadership skills
Fluent in English and French