Medical/Scientific Writer

Employment Type

: Full-Time

Industry

: Healthcare - Allied Health



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Responsibilities

  • Creates medical and scientific documents intended for submission to regulatory agencies.
  • Compiles, organizes and summarizes medical practice and clinical scientific data.
  • Writes abstracts and publications.
  • Prepares scientific and regulatory documents such as clinical protocols, investigator’s brochures, informed consent forms, annual reports, investigational new drug applications, new drug applications, regulatory correspondence, and clinical summary reports.
  • Prepares and submits annual reports, pre-clinical and clinical study reports, safety reports, and Investigator’s Brochures).
  • Performs literature searches and extracts information to support regulatory documents.
  • Prepares and edits manuscripts, meeting reports and proceedings, and safety documents.
  • Requirements

  • MSc degree or PhD.
  • Demonstrated experience in medical publishing or editing.
  • Proficient in the use of PubMed or other medical literature databases. Mastery with Microsoft Word and Excel.
  • Able to covert complex concepts into simpler messages. Has high attention to detail, is a team player and a self starter and ability to work independently.

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