Senior Staff Clinical Evaluation Specialist (Remote)

Stryker seeks a Senior Staff Clinical Evaluation Specialist to lead clinical evidence strategies and scientific documentation for surgical technologies. This remote role (Eastern/Central time zones) partners with regulatory, clinical, and commercial teams to support product development, regulatory submissions, and market access decisions.

Responsibilities

• Lead development and execution of clinical evidence strategies for new products and lifecycle management
• Manage clinical evaluation projects ensuring alignment with regulatory strategy and commercialization objectives
• Author clinical evaluations, post-market reports, safety summaries, and regulatory submission documentation
• Design and execute systematic literature reviews, synthesizing clinical and post-market data into conclusions
• Develop scientific communications including manuscripts, abstracts, presentations, and evidence materials

Requirements

• Master's degree in health, clinical, biological, biomedical science, or related field
• Minimum 6 years in clinical affairs, regulatory affairs, quality, medical writing, or medical device functions
• Minimum 2 years authoring clinical evaluations for medical devices
• Experience conducting literature reviews, evidence synthesis, and scientific data analysis
• Experience supporting regulatory submissions in healthcare industry
• Fluency in English
• Preferred: Doctoral degree (PhD, PharmD, MD) in health or science discipline

Compensation: $110,100 - $238,400 USD Annual (based on pay band)