Clinical Engineering Product Analyst Position Available In Davidson, Tennessee

Job Title:

Clinical Engineering Product Analyst Location:

Remote/Nashville Department:

Clinical Engineering /

Biomedical Technology Services Reports To:

Director of Clinical Engineering or Product Management Lead Position Summary:

The Clinical Engineering Product Analyst plays a pivotal role in supporting both the operational and research missions of a leading academic and research hospital system. This individual serves as a cross-functional resource, supporting clinical engineers, product teams, care providers, and research staff to ensure clinical technologies are safe, interoperable, and optimized for both patient care and innovation. The Analyst brings a strong understanding of medical devices and clinical workflows, paired with experience in multi-vendor environments including systems from Philips, GE, Siemens, and others. This role requires someone who is equal parts technical expert, problem-solver, and collaborator – someone who thrives in a dynamic environment where patient care, research, and clinical excellence intersect.

Key Responsibilities:

Collaborate with clinical teams, biomedical engineering, research stakeholders, and IT to support the integration, optimization, and ongoing performance of clinical technologies across the hospital system. Engage directly with care providers and researchers to understand technology needs and translate them into product or integration requirements. Analyze device and system performance data to identify trends, inefficiencies, and opportunities for improved safety, usability, and cost-effectiveness. Support device integration into EHRs (e.g., Epic), PACS, RIS, and research data systems, ensuring seamless data flow and interoperability. Serve as a subject matter expert across multiple clinical systems and platforms (e.g., GE, Philips, Siemens, Mindray, Draeger), providing hands-on support and cross-platform insight. Participate in planning, implementation, and optimization of technology rollouts across both clinical and research settings. Support vendor relationship management, including system evaluations, implementation oversight, and post-go-live support. Contribute to research initiatives requiring clinical technology data or integration, ensuring compliance with research protocols and IRB standards. Assist in compliance efforts related to Joint Commission, FDA, AAMI, and internal governance standards. Provide technical training, product documentation, and end-user support for clinical staff, product teams, and researchers.

Qualifications:

Education:

Bachelor’s degree in Biomedical Engineering, Clinical Engineering, Healthcare Technology Management, or a related field. Master’s degree in a healthcare, technical, or research-oriented discipline preferred.

Experience:

3-5+ years in a clinical engineering, healthcare technology, or product analyst role within a hospital or academic medical center. Strong working knowledge of a variety of medical device systems (e.g., Philips, GE, Siemens, Mindray, etc.). Experience collaborating with both clinical providers and research teams. Familiarity with data interoperability standards (HL7, DICOM), device integration practices, and clinical informatics.

Skills:

Excellent interpersonal communication skills and the ability to support technical and clinical end-users. Strong analytical skills and proficiency with tools such as Excel, SQL, Tableau, or equivalent. Ability to manage multiple priorities across operational and research initiatives. Strong project coordination and problem-solving abilities in complex environments.

Preferred Certifications:

Certified Clinical Engineer (CCE) Certified Biomedical Equipment Technician (CBET) Project Management Professional (PMP) ITIL, Lean, or Six Sigma certifications a plus