Senior Staff Clinical Evaluation Specialist (Remote)

Stryker; Oregon; Remote; USD 110,000 - 238,000; Full time

Job summary

Stryker is seeking a Senior Staff Clinical Evaluation Specialist for its Surgical Technologies unit. This remote US role requires residence in the Eastern or Central time zones to align with team hours.

You will lead clinical evidence strategies, manage evaluation projects, and author clinical evaluations and regulatory submissions. The position also involves mentoring cross-functional teams to improve methodologies and documentation.

Qualifications

• MS degree in health, clinical, biological, biomedical, engineering, or related field.
• At least 6 years in clinical/regulatory/quality/medical writing or related medical device functions.
• At least 2 years authoring clinical evaluations for medical devices.
• Experience with literature reviews, evidence synthesis and data analysis.
• Experience supporting regulatory submissions and lifecycle activities.
• Fluency in English.

Responsibilities

• Lead the development and execution of clinical evidence strategies for new product development and lifecycle management.
• Manage clinical evaluation projects ensuring alignment between clinical evidence, regulatory strategy, product claims, and commercialization objectives.
• Author and maintain clinical evaluations, post-market reports, safety and performance summaries, regulatory submissions, annual reports, and other clinical documentation.
• Design and execute systematic literature reviews and synthesize data into conclusions.
• Assess benefit-risk profiles and develop evidence-based regulatory considerations.
• Partner with regulatory authorities and internal stakeholders to address evidence requirements.
• Develop scientific communications including manuscripts, abstracts, presentations and customer-facing materials.
• Mentor team members and lead cross-functional review processes to improve methodologies and efficiency.

Education

Master of Science in health/science/engineering

Job description

Stryker is hiring a Senior Staff Clinical Evaluation Specialist for our Surgical Technologies business unit. This is a remote position within the United States. To align with team collaboration and business operating hours, candidates must reside in the Eastern or Central time zones.

What You Will Do

• Lead the development and execution of clinical evidence strategies for new product development and lifecycle management activities.
• Manage clinical evaluation projects, ensuring alignment between clinical evidence, regulatory strategy, product claims, and commercialization objectives.
• Author and maintain clinical evaluations, post-market clinical follow-up reports, safety and performance summaries, regulatory submissions, annual reports, and other clinical documentation.
• Design and execute systematic literature reviews, evaluate published evidence, and synthesize clinical, preclinical, and post-market data into scientifically supported conclusions.
• Assess benefit-risk profiles of medical devices and develop evidence-based recommendations in accordance with global regulatory requirements.
• Partner with regulatory authorities and internal stakeholders to address clinical evidence requirements and support regulatory submissions.
• Develop scientific communications, including manuscripts, conference abstracts, presentations, white papers, and customer-facing evidence materials.
• Mentor team members, lead cross-functional review processes, and identify opportunities to improve clinical evaluation methodologies, documentation practices, and team efficiency.

What You Need

Required

• Master of Science degree in a health, clinical, biological science, biomedical, engineering, or related scientific field.
• Minimum 6 years of experience in clinical affairs, regulatory affairs, quality, medical writing, clinical evaluation, post-market surveillance, or related medical device functions.
• Minimum 2 years of experience authoring clinical evaluations for medical devices.
• Experience conducting literature reviews, evidence synthesis, and scientific analysis using clinical and technical data.
• Experience supporting regulatory submissions and product lifecycle activities within a regulated healthcare industry.
• Fluency in English.

Preferred

• Doctoral degree (PhD, PharmD, MD, or equivalent) in a health or science-related discipline.
• Experience supporting global medical device regulatory requirements, including clinical evaluation, post-market surveillance, and market access activities.
• Experience developing scientific publications, conference presentations, and clinical evidence communication strategies.
• Experience managing complex cross-functional projects within the medical device industry.

Posted Date: 10/01/2026

This role will be posted for a minimum of 3 days.

United States of America Pay Ranges:

• USN: $110,100 - $183,400 USD Annual
• US5: $115,600 - $192,600 USD Annual
• US10: $121,100 - $201,700 USD Annual
• US15: $126,600 - $210,900 USD Annual
• US20: $132,100 - $220,100 USD Annual
• US30: $143,100 - $238,400 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.