Sr Clinical User Experience Specialist

Siemens Healthineers • Greendale, WI

7d • Remote

About The Position

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Who we are: We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways. How we work: When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Requirements

• six (6) years of experience in the job offered (no degree), as Design Validation Specialist, Lead Radiation Therapist, Radiation Oncology Faculty, or a related occupation.
• Must have experience and/or academic training with each of the following:
• Comprehensive understanding of radiation therapy clinical workflows
• Patient care, positioning & safety, treatment planning & delivery
• Proficient and efficient use of linear accelerators such as 21EX, 2300 IX/Trilogy, TrueBeam
• Experience performing advanced radiotherapy techniques, such as IMRT, VMAT, SRS and SBRT
• Knowledge of the ARIA radiation therapy management and Eclipse treatment planning applications

Responsibilities

• Enhance the team's clinical expertise by developing educational materials, conducting hands-on and remote training sessions, and leading customer site visits.
• Collaborate on the creation of human factors validation plans and clinically relevant test scripts, while supporting researchers in conducting user testing.
• Offer subject matter expertise and valuable insights during the initial stages of product development.
• Guide design decisions by serving as the voice of the customer throughout the entire product development process.
• Ensure medical devices meet quality standards and user needs while minimizing risks.
• Follow FDA & European CE standards for medical device/product development validation.
• Ensure that medical devices being developed are of high quality and conform to the defined use needs and intended uses, while minimizing use related risks.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees