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