Remote QC Editor – Medical Writing

BeOne Medicines Ltd.

United States

On-site

USD 75,000 - 100,000

Full time

4 days ago
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Job summary

BeOne Medicines is seeking a QC Specialist to coordinate and complete QC reviews of clinical and regulatory documents, ensuring accuracy, data verification, and proper formatting under strict timelines.

The role involves remote work or from BeOne’s global offices, with emphasis on cross-referencing, testing hyperlinks, and ensuring compliance with FDA/ICH guidelines. Strong English communication and attention to detail are essential.

Qualifications

  • Experience performing medical writing QC reviews of regulatory documents (e.g., study reports, protocols, amendments).
  • Familiarity with FDA regulations and ICH guidelines for regulatory submissions.
  • Strong attention to detail, grammar, and scientific accuracy in technical documents.
  • Excellent written and spoken English communication and collaboration within teams.

Responsibilities

  • Coordinate QC reviews for clinical/regulatory documents within tight timelines.
  • Perform cross-referencing, fact-checking, data verification, and proofreading.
  • Ensure compliance with Global Medical Writing conventions, templates, and regulatory guidelines.
  • Collaborate with Medical Writers and other internal teams to meet deliverables.

Skills

Quality control
Medical writing QC
Regulatory submissions
Fact-checking
English communication

Education

BA/BS degree
Advanced degree a plus

Tools

Microsoft Word
Microsoft Excel
PowerPoint
Adobe Acrobat
SharePoint
Veeva Vault

Job description

BeOne Medicines is seeking a QC Specialist to coordinate and complete QC reviews of clinical and regulatory documents, ensuring accuracy, data verification, and proper formatting under strict timelines.

The role involves remote work or from BeOne’s global offices, with emphasis on cross-referencing, testing hyperlinks, and ensuring compliance with FDA/ICH guidelines. Strong English communication and attention to detail are essential.

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