Clinical Evidence Planning & Evaluations Manager

Siemens Healthineers

Clinical evidence manager developing evaluations and post-market follow-up for Varian medical devices at Siemens Healthineers. Supporting regulatory, product-management, and promotional-content decisions.

Posted 8/17/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSenior💰 $134,300 - $184,668 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in developing Clinical Evaluation Plans and Reports, with a strong understanding of Clinical Evaluation and Post-Market Clinical Follow-Up requirements for medical devices. Possesses exemplary technical writing and communication skills, essential for cross-functional collaboration and customer-facing content review.

Highest-signal resume keywords

Clinical Evaluation Plans DevelopmentPost-Market Clinical Follow-Up ActivitiesTechnical Writing SkillsMedical Device Regulations KnowledgeClinical Evaluations Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Evaluation ReportsPost-Market Clinical Evaluation PlansPost-Market Clinical Evaluation ReportsRisk ManagementClinical StudiesCustomer SurveysLiterature SearchesMedical PhysicsBiomedical Engineering

Soft Skills

Verbal Communication Skills

Certifications & Qualifications

Master’s or PhD in Medical PhysicsPhD in BiophysicsPhD in Biomedical Engineering

Industry Keywords

Medical DevicesRadiation OncologyEU MDRClass I–III Medical DevicesControlled TechnologyUS Export Control Law

About the role

Key responsibilities & impact

Create and drive clinical evidence strategies for Varian’s devices
Develop Clinical Evaluation Plans, Clinical Evaluation Reports, Post-Market Clinical Evaluation Plans, and Post-Market Clinical Evaluation Reports
Provide clinical perspective and input to cross-functional teams on clinical development, risk management, product management, and post-market surveillance
Execute Post-Market Clinical Follow-Up activities, including customer surveys, annual literature searches, and clinical studies
Review promotional material and claims supporting customer-facing content

Requirements

What you’ll need

Familiarity with the design and manufacture of medical devices, especially radiation oncology devices
Exemplary technical writing and verbal communication skills
Understanding of Clinical Evaluation and Post-Market Clinical Follow-Up requirements for Class I–III medical devices under the EU MDR
Master’s or PhD in Medical Physics, Biophysics, Biomedical Engineering, or another degree program considered based on experience
3–5 years’ experience with clinical evaluations, medical physics, or a related field
Ability to work with controlled technology in accordance with US export control law

Benefits

Comp & perks

Flexible and dynamic work environment
Professional and personal growth opportunities
Medical insurance
Dental insurance
Vision insurance
401(k) retirement plan
Life insurance
Long-term and short-term disability insurance
Paid parking/public transportation
Paid time off
Paid sick and safe time