Clinical Engineering Product Analyst Job at Medasource, Nashville, TN

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  • Medasource
  • Nashville, TN

Job Description

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

Job Tags

Remote job,

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