Medical Writer

il y a 2 jours


Paris, France Cmed Temps plein

Cmed is seeking a Medical Writer with regulatory medical writing experience for this client dedicated opportunity. Experience with at least 2 of the documents: abbreviated protocol, protocol, and subsequent amendments, amended protocols, clinical study reports (all phases), lay summary of results, narratives, Clinical modules of CTDs, Q&A, P70, investigators brochures, CTAs, IND/IMPDS, benefit risk assessment. Clinical development and/or coordination of clinical activities is an asset.


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