Regulatory Content Manager

3 days ago


Liverpool, Liverpool, United Kingdom Life Sciences Recruitment Full time

**Key Responsibilities**

  • Prepare clinical regulatory documents, including Clinical Study Protocols, Clinical Study Reports, and Investigator Brochures.
  • Oversee and coordinate other writers and QC specialists assisting on documents under your responsibility.
  • Ensure timely delivery of documents and manage project budgets.
  • Work closely with clients and authors to coordinate review cycles, meetings, and project timelines.

**Requirements**

  • At least 3 years of experience actively writing regulatory documents.
  • Experience working as a lead writer on complex projects.
  • Strong understanding of clinical regulatory documents and industry standards.
  • Excellent communication and interpersonal skills.
  • Ability to work under tight deadlines and prioritize tasks effectively.

**Compensation**

The estimated salary for this position is $120,000 - $150,000 per year, depending on experience.



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