Senior Clinical Evaluation Specialist (Remote) jobs in United States
cer-icon
Apply on Employer Site
company-logo

Stryker · 20 hours ago

Senior Clinical Evaluation Specialist (Remote)

Stryker Corporation is a leading medical technology company, and they are seeking a Senior Clinical Evaluation Specialist to establish evaluation strategies and compile clinical evidence for medical devices. This role involves supporting clinical evidence strategies throughout the product development cycle and analyzing relevant data from multiple sources.

BiotechnologyHealth CareLife ScienceMedicalMedical Device
check
Growth Opportunities
check
H1B Sponsor Likelynote

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

Qualification

Clinical evaluationRegulatory affairsProject managementScientific writingData analysisInfluencing skillsCommunication skills

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

Bonus eligible
Benefits

Company

Stryker is a medical technology company that offers products and services in orthopaedics.

H1B Sponsorship

Stryker has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (105)
2024 (76)
2023 (63)
2022 (78)
2021 (57)
2020 (77)

Funding

Current Stage
Public Company
Total Funding
unknown
1990-01-02IPO

Leadership Team

leader-logo
Kevin Lobo
Chair & CEO
linkedin
leader-logo
Glenn S. Boehnlein
Chief Financial Officer and Vice President
linkedin
Company data provided by crunchbase