Freelance Writer

1 month ago


Kuwait City 44 Clinical Full time
  • Proven experience as a regulatory writer in the life sciences sector (biotech, pharma, or medical devices).
  • Expertise in regulatory submission processes for major markets (FDA, EMA, or other global agencies).
  • Strong ability to write and edit regulatory documents with a high level of accuracy and attention to detail.
  • Familiarity with Good Clinical Practice (GCP) and Good Documentation Practice (GDP).
  • Degree in life sciences, pharmacy, medicine, or a related field. Advanced degrees or certifications (e.g., RAC) are a plus.


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