
10,000+ employees
🏥 Healthcare
⚕️ Healthcare Insurance
🧬 Biotechnology
💰 $1.5M Grant on 2021-05
Healthcare • Healthcare Insurance • Biotechnology
Siemens Healthineers is a leading MedTech company focused on pioneering breakthroughs in healthcare. They offer a comprehensive portfolio that addresses the entire care continuum for serious diseases, including medical imaging, laboratory diagnostics, point-of-care testing, and digital health solutions. With a commitment to innovation, sustainability, and improving patient access to care, Siemens Healthineers collaborates with healthcare professionals and organizations globally to advance medical technology and enhance patient outcomes.
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10,000+ employees
🏥 Healthcare
⚕️ Healthcare Insurance
🧬 Biotechnology
💰 $1.5M Grant on 2021-05
Healthcare • Healthcare Insurance • Biotechnology
Siemens Healthineers is a leading MedTech company focused on pioneering breakthroughs in healthcare. They offer a comprehensive portfolio that addresses the entire care continuum for serious diseases, including medical imaging, laboratory diagnostics, point-of-care testing, and digital health solutions. With a commitment to innovation, sustainability, and improving patient access to care, Siemens Healthineers collaborates with healthcare professionals and organizations globally to advance medical technology and enhance patient outcomes.
• 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
• 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
• 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
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