Manager, Medical Writing - Remote

Overview

The Manager, Medical Writing will lead various medical writing projects across Nuvalent’s growing clinical pipeline and strengthen the company’s medical writing capabilities and quality standards.

In Short

• Prepare and finalize clinical documents such as study protocols and clinical study reports.
• Identify and champion process improvements for Medical Writing efficiencies.
• Lead medical writing projects, including scheduling and tracking.
• Collaborate with cross-functional colleagues to create clear scientific documents.
• Oversee consultant writers and provide peer review of deliverables.
• Maintain knowledge of industry and regulatory guidelines.
• Strong written/verbal communication skills are essential.
• Ability to manage multiple projects and deadlines effectively.
• Lead and mentor a team of writers.
• Oncology experience is preferred.

Requirements

• Experience as lead writer for clinical and regulatory documents.
• Advanced degree preferred.
• 3-5 years’ experience in clinical and regulatory medical writing.
• In-depth understanding of regulatory standards.
• Excellent interpersonal skills to communicate effectively.

Benefits

• Equal employment opportunities for all employees.
• Supportive work environment with professional development.