This Clinical Evidence Planning and Evaluations Manager role leads clinical evidence strategy and supports clinical evaluations, post-market clinical follow-up, and claims review for Varian devices in radiation oncology and interventional oncology. The position requires strong clinical, regulatory, and technical writing expertise to partner cross-functionally across product development, risk management, post-market surveillance, and customer-facing content. As a Clinical Evidence Planning and Evaluations Manager, you will: • Develop and execute clinical evidence strategies for Software as a Medical Device (SaMD), digital health, and AI-enabled solutions across the product lifecycle. • Author and maintain Clinical Evaluation Plans and Reports (CEP/CER) and Post-Market Clinical Follow-up Plans and Reports (PMCFP/PMCFR) to support global regulatory compliance and market access. • Partner with Regulatory Affairs, Quality, Product Management, Risk Management, Engineering, and Medical Affairs to define and address clinical evidence requirements. • Lead evidence generation activities, including literature evaluations, clinical performance assessments, real-world evidence analyses, and post-market surveillance initiatives. • Support clinical benefit-risk assessments, intended use validation, and product claims substantiation. • Monitor post-market clinical data and emerging evidence to identify gaps, risks, and opportunities for continuous improvement. This position may be a good fit if you: • Have experience with Software as a Medical Device (SaMD), digital health technologies, AI-enabled medical devices, or healthcare software solutions. • Understand clinical evidence generation, clinical performance evaluation, and post-market surveillance principles. • Possess strong scientific writing, critical analysis, and communication skills. • Thrive in a collaborative, cross-functional environment while working independently in a remote setting. Required qualifications • Working knowledge of Clinical Evaluation and Post-Market Clinical Follow-up requirements under the European Union Medical Device Regulation (EU MDR), particularly for software-based medical devices. • Master's degree or higher in Biomedical Engineering, Medical Physics, Computer Science, Health Sciences, Public Health, Biostatistics, or a related field; equivalent experience will be considered. • 3+ years of experience in clinical evaluation, clinical evidence generation, medical devices, SaMD, digital health, or a related field. • Experience evaluating clinical data, scientific literature, and real-world evidence to support regulatory and business objectives. • Familiarity with AI/ML-enabled medical technologies, clinical performance validation, and software lifecycle processes is preferred. #LI-Remote The expected compensation for this position is: $93,000 - $132,500 Factors which may affect starting compensation within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. Siemens Healthineers offers a variety of health and wellness benefits including a flexible benefits plan, Defined Contribution Pension Plan, Registered Retirement Savings Plan matching contributions, plus a competitive paid time off program including vacation, company holidays, sick leave, and parental leave (all subject to eligibility requirements). This information is provided per required laws and regulations. Applicants should apply via Siemens Healthineers external or internal careers site.