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Medical Technical Writer

OnTarget Communications Netanya, Center District, Israel

Staffing and Recruiting · 1 employee

20 h ago
technical-writer Mid (2-5 yrs) Full-time Israel
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About the role

The role involves writing and editing clinical and regulatory documents such as protocols, CSRs, and IBs while ensuring compliance with international standards. You will also lead document development cycles and translate complex scientific data into clear, accurate content for global teams.

What they look for

Medical writing Clinical documentation Regulatory documentation Scientific writing Protocol development CSR writing IB writing Regulatory guidelines Data analysis MS Word Technical writing Communication Editing Regulatory compliance

Requirements

Candidates must hold a degree in life sciences and possess at least 4 years of experience in clinical or regulatory medical writing. Proficiency in MS Word and exceptional English communication skills are required to manage submissions and regulatory guidelines.

Full description

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

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