Clinical Evidence Planning & Evaluations Manager

This is a fully remote position, open to applicants in United States, +1 more country.

📋 Description

• Develop and implement clinical evidence strategies for Varian’s devices.

• Create Clinical Evaluation Plans, Clinical Evaluation Reports, Post-Market Clinical Evaluation Plans, and Post-Market Clinical Evaluation Reports.

• Offer clinical insights and contributions to cross-functional teams regarding clinical development, risk management, product management, and post-market surveillance.

• Conduct Post-Market Clinical Follow-Up activities, which include customer surveys, annual literature reviews, and clinical studies.

• Evaluate promotional materials and claims that support customer-facing content.

⛳️ Requirements

• Knowledge of the design and production of medical devices, particularly in radiation oncology.

• Outstanding technical writing and verbal communication abilities.

• Familiarity with Clinical Evaluation and Post-Market Clinical Follow-Up requirements for Class I–III medical devices as per the EU MDR.

• A Master’s or PhD in Medical Physics, Biophysics, Biomedical Engineering, or a related degree considered based on experience.

• 3–5 years of experience in clinical evaluations, medical physics, or a related discipline.

• Capability to work with controlled technology in compliance with US export control laws.

🏝️ Benefits

• Flexible and dynamic work environment.

• Opportunities for professional and personal development.

• 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.