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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 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
  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Industries

    Hospitals and Health Care

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