Manager, Medical Writing

Stryker • Portland, OR

2d • $126,500 - $273,900 • Remote

About The Position

Stryker is hiring a Manager, Medical Writing for our Endoscopy division. This is a remote position based in the United States. As the Manager, Medical Writing you will support clinical evaluation and regulatory documentation across a diverse endoscopy portfolio. In this role, you will lead a distributed team, oversee end-to-end medical writing deliverables, and contribute scientific expertise throughout the product lifecycle. The position interfaces closely with clinical, regulatory, quality, and commercial teams to ensure compliant, high-quality outputs across regions.

Requirements

• Bachelor’s degree in life sciences, biology, biomedical engineering, nursing, or related discipline
• Minimum 8 years of experience in medical writing, clinical research, or related field
• Minimum 2 years of people management experience or leadership of critical projects
• Demonstrated experience authoring regulatory and clinical evaluation documents (e.g., clinical evaluation reports, study reports, literature summaries)

Nice To Haves

• Advanced degree (Master’s or higher) in a relevant field
• Certification in clinical research or project management
• Minimum 2 years of experience in the medical device industry or pharmaceutical industry
• Experience applying global regulatory requirements, including ISO, FDA, and international regulations

Responsibilities

• Lead and manage a global team of medical writers, including hiring, onboarding, performance management, and development against defined performance metrics
• Oversee delivery of clinical evaluation documents, including protocols, reports, literature reviews, and post-market documentation, ensuring on-time completion and regulatory compliance
• Plan and allocate resources to meet project timelines, tracking key performance indicators for quality, timeliness, and productivity
• Direct development of clinical study protocols, clinical study reports, manuscripts, and scientific publications in alignment with clinical and regulatory requirements
• Apply regulatory standards (ISO, FDA, international regulations) to writing strategies and documentation across product development stages
• Establish and maintain standardized processes, templates, and tools to improve efficiency, consistency, and audit readiness
• Partner with cross-functional stakeholders to align priorities, support product development, and ensure accuracy of clinical and promotional claims
• Manage budgets, forecasts, and operational metrics, and implement process improvements including automation and standardization initiatives

Benefits

• USN: $126,500 - $210,700 USD Annual
• US5: $132,800 - $221,200 USD Annual
• US10: $139,200 - $231,800 USD Annual
• US15: $145,500 - $242,300 USD Annual
• US20: $151,800 - $252,800 USD Annual
• US30: $164,500 - $273,900 USD Annual
• View the U.S. work location and transparency guide to find the pay range for your location.
• Travel Percentage: 10%

What This Job Offers

• Job Type: Full-time
• Career Level: Manager