Manager, Medical Writing

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.

What You Will Do

• 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

What You Need

Required

• 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)

Preferred

• 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

Posted Date: 06/25/2026
This role will be posted for a minimum of 3 days.

United States of America Pay Ranges:

• 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.

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.