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Medical Technical Writer
OnTarget Communications β’ Remote/Nationwide
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Location: Netanya
Model: Onsite
Scope: Fulltime - Employed
Description: We are looking for a fullβtime 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 highβquality 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
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Mid-Senior level
Full-time
Hospitals and Health Care