Medical editor and proofreader for clinical research

Company: We are a quality control provider for pharmaceutical companies and clinical research organizations (CROs), specializing in the editing of clinical trial documentation for regulatory submission.

Responsibilities:

• Edit and proofread clinical study protocols, informed consent forms (ICFs), and clinical study reports (CSRs).
• Verify the accuracy and consistency of medical terminology, statistical data, and formatting across all document sections.
• Ensure all documents comply with specific style guides (AMA, ICH) and internal quality checklists.
• Manage multiple editing projects simultaneously, adhering to strict client deadlines.
• Provide clear, actionable feedback using Microsoft Word's track changes and comment functions.

Requirements:

• Minimum of 2 years of direct experience editing clinical research or regulatory documents.
• Educational background in life sciences (e.g., Biology, Pharmacology, Nursing).
• Expert proficiency with Microsoft Word, including advanced style and formatting tools.
• Meticulous attention to detail and a commitment to producing error-free work.
• Ability to work independently in a remote setting with highly confidential information.