Medical Technical Writer

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. Qualifications Degree in life sciences 4+ years of medical writing experience in clinical/regulatory environments Solid writing and editing skills of clinical regulatory documents Excellent scientific writing, editing, and communication skills Familiarity with global regulatory guidelines Proficiency in MS Word English MT level - exceptional written and spoken communication