Principal Regulatory Writer

3 weeks ago


Liverpool, Liverpool, United Kingdom Life Sciences Recruitment Full time
Principal Regulatory Writer Job Opportunity:

Join our esteemed organization as a Principal Regulatory Writer, where you'll be responsible for preparing high-quality clinical regulatory documents that comply with regulatory requirements.

About the Role:

You will:

  • Develop and execute comprehensive plans for document production, ensuring timely completion and meeting budget objectives.
  • Liaise with clients to understand their needs, provide expertise on document content, and facilitate seamless communication among team members.
  • Ensure consistency in document style, formatting, and content across all projects.
  • Stay current with evolving regulatory landscapes and industry developments, applying this knowledge to enhance document quality and compliance.
Requirements and Qualifications:
  • Minimum 3 years of experience in regulatory writing, with a strong focus on clinical documents.
  • Experience in leading cross-functional teams and collaborating with clients to deliver high-quality documents.
  • Degree in science/pharmacy (Postgraduate qualifications advantageous).
  • Outstanding written and verbal communication skills.
  • Ability to juggle multiple projects, meet deadlines, and adapt to changing priorities.
Estimated Salary:

$130,000 - $160,000 per annum.



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