Contract Medical Writer (QC/Copy Editing Focus)

Position Overview

We are collaborating with a cutting-edge biopharmaceutical company specializing in central nervous system (CNS) disorders to hire a contract Medical Writer. This role deviates from typical authoring responsibilities, emphasizing quality control (QC) reviewing of clinical and regulatory documentation. The focus is on verifying accuracy, consistency, formatting, grammar, and compliance before document finalization.

Key Responsibilities

• Perform comprehensive quality control reviews of clinical and regulatory documents to ensure error-free content.
• Maintain consistency and adherence to formatting and compliance standards across various medical documents.
• Apply strong editing and copy editing skills to enhance document clarity and precision.
• Work independently to manage QC tasks efficiently within a dynamic, fast-paced environment.

Qualifications

• Prior experience in medical writing within the pharmaceutical or biotechnology sectors is essential.
• Proven background in quality control review, copy editing, or document quality assurance.
• Keen eye for detail combined with strong editing capabilities.
• Familiarity with clinical and regulatory document types relevant to medical writing.
• Ability to operate autonomously and manage time effectively.

Additional Information

• Position is fully remote, available to candidates residing in the United States.
• Contract-based employment opportunity.
• Workload varies between approximately 15 to 40 hours weekly depending on project demands.
• Ideal for professionals seeking flexible contract roles focusing on editorial and quality review functions of medical writing.