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 and Reports as well as Post-Market Clinical Evaluation Plans and Reports (CEP/CER and PMCFP/PMCFR).

• Offer clinical insights and contributions to cross-functional teams involved in 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.

• Assess promotional materials and claims for customer-facing communications.

• Enhance the influence of Medical Affairs initiatives throughout the organization.

⛳️ 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 regulations for Class I–III medical devices under the EU MDR.

• Master’s or PhD in Medical Physics (preferred), Biophysics, Biomedical Engineering; other relevant degrees may be considered based on experience.

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

• Capability to work remotely from the United States or Canada.

• Proficiency in handling controlled technology in compliance with US export control laws.

🏝️ Benefits

• 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.

• Flexible and dynamic work environment.

• Resources and flexibility for professional and personal development.