Senior Clinical Document Coordinator

4 days ago

Sydney, New South Wales, Australia beBeeMedical Full time $100,000 - $140,000
Regulatory Medical Writer Opportunity

We are seeking an experienced regulatory medical writer to fill this key role. This is a remote, hybrid or office-based opportunity.

About the Position:

You will be responsible for coordinating and writing clinical study documents, including investigator brochures, clinical study protocols, participant information and consent forms, and clinical study reports.

Key Responsibilities:
  • Coordinate and write clinical study documents
  • Edit and review clinical study documents
  • Mentor junior medical writers
  • Ensure quality processes are maintained
Requirements:
  • Bachelor's degree in a scientific or relevant field
  • Possession of a higher degree in a scientific or relevant field (desired)
  • A minimum of two years' experience as a medical writer
  • Familiarity with ICH GCP guidelines, ICH E3 guidelines, medical terminology, and clinical trials processes
  • Excellent communication and organizational skills

This role offers excellent opportunities for professional growth and development. If you are a highly skilled medical writer looking for a new challenge, please apply for this exciting opportunity.

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