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

📋 Description

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

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

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

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

• Evaluate promotional materials and claims to ensure accuracy in customer-facing content.

⛳️ Requirements

• Knowledge of the design and manufacturing processes for medical devices, particularly those utilized in radiation oncology.

• Strong technical writing and verbal communication abilities.

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

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

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

• Capability to work independently in a remote setting.

• Travel requirement is less than 25%.