Clinical Evidence Planning & Evaluations Manager

About the role

This role will lead the planning and execution of clinical evidence activities that support medical device development, regulatory submissions, and post-market readiness. The ideal candidate will partner closely with regulatory, product management, and cross-functional stakeholders to shape evidence strategies and ensure clinical claims are supported by robust documentation. This position will also play a key role in post-market clinical follow-up efforts and the review of external-facing materials for clinical accuracy.

Responsibilities

• Develop and implement clinical evidence strategy for the company's devices
• Create clinical evaluation plans and reports, including PMCF plans and reports
• Provide clinical input to regulatory and product management teams
• Conduct post-market clinical follow-up activities, including customer surveys and literature searches
• Review promotional materials and claims for clinical accuracy

Qualifications

• Master’s or PhD in Medical Physics, Biophysics, Biomedical Engineering, or relevant experience
• 3-5 years of experience in clinical evaluations or medical physics
• Strong understanding of EU MDR requirements for medical devices
• Exemplary technical writing and verbal communication skills
• Familiarity with medical devices used in radiation oncology

Benefits

• Medical, dental, and vision insurance
• 401(k) retirement plan
• Life insurance coverage
• Long-term and short-term disability insurance
• Paid time off and sick leave
• Paid public transportation or parking

Pay

$134,300 – $184,668 annually

Schedule

Remote – US based candidates only, no visa sponsorship available