Senior Clinical Evaluation Lead – Remote

Stryker Corporation; Portage (MI); Remote; USD 132,000 - 238,000; Full time

Job summary

Stryker Corporation in the United States seeks a Senior Staff Clinical Evaluation Specialist to lead clinical evidence strategies for Surgical Technologies. The role is remote with residency in Eastern/Central time zones to align with team hours.

You will manage clinical evaluation projects, author evaluations and reports, and collaborate with regulatory and commercial teams to ensure compliant, evidence-based product development and lifecycle management.

Qualifications

• Master's degree in a health/clinical/biological science or engineering field is required.
• Doctoral degree (PhD/ PharmD/ MD or equivalent) is preferred.
• Minimum 6 years in clinical affairs, regulatory, quality, medical writing, or related medical device functions.
• Minimum 2 years authoring clinical evaluations for medical devices.

Responsibilities

• Lead clinical evidence strategies for new products and lifecycle management.
• Manage clinical evaluation projects aligning evidence, regulatory strategy, claims and commercialization.
• Author and maintain clinical evaluations, post-market reports and regulatory submissions.
• Design literature reviews, evaluate evidence, and synthesize data into conclusions.
• Assess benefit-risk and develop evidence-based regulatory recommendations.
• Collaborate with regulatory authorities and internal stakeholders on evidence needs.
• Develop scientific communications such as manuscripts, abstracts, presentations.
• Mentor teammates and improve evaluation methodologies and processes.

Skills

Fluent English

Education

Master of Science in health/clinical/biological science/biomedical/engineering or related field

Doctoral degree (PhD, PharmD, MD, or equivalent)

Job description

Stryker Corporation in the United States seeks a Senior Staff Clinical Evaluation Specialist to lead clinical evidence strategies for Surgical Technologies. The role is remote with residency in Eastern/Central time zones to align with team hours.

You will manage clinical evaluation projects, author evaluations and reports, and collaborate with regulatory and commercial teams to ensure compliant, evidence-based product development and lifecycle management.