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