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Regulatory Document Writer

3 weeks ago

Cork, Cork, Ireland beBee Careers Full time
About the Role

This is a contract role requiring a highly skilled Regulatory Document Writer to create high-quality documents for external scientific publications and regulatory submissions.

Key Responsibilities
  • Write, edit, and review documents to ensure accuracy and quality.
  • Facilitate trial development and product registration by coordinating with cross-functional teams.
  • Maintain and enhance therapeutic area knowledge, including disease state and compound information.
  • Develop and prepare presentations for internal and external stakeholders.
Requirements
  • Bachelor's Degree or higher in a relevant field.
  • Graduate degree with formal research component or in life sciences.
  • Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience.
  • Publication experience and ability to work well independently.