No longer accepting applications (expired, filled, etc.)
Stryker
Senior Clinical Evaluation Specialist (Remote)
The Senior Clinical Evaluation Specialist applies scientific, regulatory, and project management skills to establish evaluation strategies and compile clinical evidence to reach legally binding conclusions on the safety and performance of medical devices throughout their lifecycle. This role supports a coherent clinical evidence strategy across new product development and aligns with marketing, regulatory, clinical research, and testing strategies.
Key Responsibilities
- • Support a coherent clinical evidence strategy throughout the new product development cycle, and foster alignment with adjacent complex processes (marketing strategy and claims, regulatory strategy, clinical research strategy, testing strategy).
- • Support compliant and sustainable literature search strategies, and perform complex literature queries to retrieve published clinical data.
- • Identify, appraise, and analyze all relevant data (clinical, PMS, marketing, testing, etc.) from multiple sources and formats and create a comprehensive scientific review.
- • Analyze the current medical and scientific trends in the clinical state of the art on a broad variety of specialized indications and techniques.
- • Identify unanswered questions and residual risks in the clinical evaluation report, and assist with design of Post Market Clinical Follow Up (PMCF) activities in collaboration with clinical affairs colleagues and/or other subject matter experts to address these questions.
- • Define and develop clinical evaluation and analysis methodologies to adapt to a complex and quickly evolving regulatory and scientific framework.
Required
- • A minimum of a bachelor’s degree in a technical and/or scientific discipline required.
- • Minimum of 2 years industry experience in clinical, quality or regulatory affairs (Risk Management, Design quality, Post Market Safety etc.).
- • Strong communication, project management and influencing skills. Must demonstrate the ability to effectively communicate up/down and across different levels of the organization.
- • Ability to travel domestically and internationally, up to 20%.
Preferred
- • Master’s or Ph.D. or other higher degree in health-related field (RN, BSN, BPharm/MD/MPH).
- • Experience in scientific or medical writing, relevant academic or clinical research experience (PhD, Post-doc).
- • Good working understanding of regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
- • Good working knowledge of areas linked to clinical evaluation (e.g. regulatory requirements, data analysis, critical appraisal etc.).
- • Successful track record in managing complex deliverables independently and managing simple projects.
- • Ability to follow internal procedures and processes and contribute with suggestions for improvements.
Benefits & Perks
- • Medical and prescription drug insurance
- • Dental insurance
- • Vision insurance
- • Critical illness insurance
- • Accident insurance
- • Hospital indemnity insurance
- • Personalized healthcare support
- • Wellbeing program
- • Tobacco cessation program
- • Health Savings Account (HSA)
- • Flexible Spending Accounts (FSAs)
- • 401(k) plan
- • Employee Stock Purchase Plan (ESPP)
- • Basic life and AD&D insurance
- • Short-term disability insurance
Company Overview
Industry: Healthcare Technology
Company Size: 500-1,000 employees
Founded: 2015
Headquarters: San Francisco, CA
Company Links
Key Contacts
Contact information not available
About the Company
Leading healthcare technology company focused on improving patient outcomes through innovative digital solutions. We're transforming the way healthcare is delivered with cutting-edge technology and data-driven insights. Our platform serves over 10,000 healthcare professionals and has processed millions of patient interactions.
Recent News & Updates
Series B
Raised $50M Series B funding - Jan 2024
Award
Named "Best Healthcare Startup" by TechCrunch - Dec 2023
Growth
Expanded to 5 new states - Nov 2023
The Senior Clinical Evaluation Specialist applies scientific, regulatory and project management skills to establish the evaluation strategy and compile a body of clinical evidence, in order to reach a legally binding scientific conclusion on the safety and performance of medical devices throughout the product lifecycle. This role is Remote supporting our Instruments Division, with preference to candidates in the Eastern United States.
What You Will Do
Posted Date: 01/27/2026 This role will be posted for a minimum of 3 days.
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.
What You Will Do
- Support a coherent clinical evidence strategy throughout the new product development cycle, and foster alignment with adjacent complex processes (marketing strategy and claims, regulatory strategy, clinical research strategy, testing strategy).
- Support compliant and sustainable literature search strategies, and perform complex literature queries to retrieve published clinical data,
- Identify, appraise, and analyze all relevant data (clinical, PMS, marketing, testing, etc.) from multiple sources and formats and create a comprehensive scientific review.
- Analyze the current medical and scientific trends in the clinical state of the art on a broad variety of specialized indications and techniques.
- Identify unanswered questions and residual risks in the clinical evaluation report, and assist with design of Post Market Clinical Follow Up (PMCF) activities in collaboration with clinical affairs colleagues and/or other subject matter experts to address these questions.
- Define and develop clinical evaluation and analysis methodologies to adapt to a complex and quickly evolving regulatory and scientific framework.
- A minimum of a bachelor’s degree in a technical and/or scientific discipline required.
- Minimum of 2 years industry experience in clinical, quality or regulatory affairs (Risk Management, Design quality, Post Market Safety etc.).
- Strong communication, project management and influencing skills. Must demonstrate the ability to effectively communicate up/down and across different levels of the organization.
- Ability to travel domestically and internationally, up to 20%.
- Master’s or Ph.D. or other higher degree in health-related field (RN, BSN, BPharm/MD/MPH).
- Experience in scientific or medical writing, relevant academic or clinical research experience (PhD, Post-doc).
- Good working understanding of regulations, technical standards, guidance documents, test reports, clinical and medical terminology, technical product information, and complex documents.
- Good working knowledge of areas linked to clinical evaluation (e.g. regulatory requirements, data analysis, critical appraisal etc.).
- Successful track record in managing complex deliverables independently and managing simple projects.
- Ability to follow internal procedures and processes and contribute with suggestions for improvements.
- $ 83,300.00 - $138,800.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.
Posted Date: 01/27/2026 This role will be posted for a minimum of 3 days.
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.
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