About this role
Location: Netanya Model: Onsite Scope: Fulltime - Employed Description: We are looking for a full‑time Medical Writer for a multinational organization Responsibilities Write and edit clinical and regulatory documents (protocols, CSRs, IBs, summaries). Translate complex scientific data into clear, compliant content. Lead document development and review cycles across global teams. Ensure accuracy, consistency, and alignment with international regulatory standards. Manage timelines and deliver high‑quality submissions.