QC Editor/Publisher

The Quality Control Editor position at ProPharma Group is responsible for ensuring the accuracy and quality of clinical documents, regulatory submissions, and medical publications.

Key Responsibilities:

• Perform detailed quality reviews of clinical, nonclinical, and regulatory documents to verify content accuracy and consistency.
• Interpret clinical data and literature to perform quality control duties.
• Proofread and edit documents to correct grammar, spelling, punctuation, style, and format.
• Verify document content consistency with internal, client, and related authority guidelines.
• Format, style, and troubleshoot document functionality and presentation.
• Ensure compliance with document format per templates and style guides.
• Lead resolution of discrepant findings within documents.
• Possess knowledge of AMA Manual of Style and other style guides.

Requirements:

• Excellent use of the English language.
• Expertise in Microsoft Word and understanding of Acrobat/PDF software.
• Excellent language skills (reading, writing, editing, team communication).
• Pharmaceutical and/or Biotech background strongly preferred.
• Exceptional time management skills and attention to detail.

Educational and Experience Requirements:

• College degree or 2+ years of education in a related field.
• At least 3 years of QC/editing-related job history.