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Clinical Specialist

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: MediView XR, Inc.
Full Time position
Listed on 2026-01-25
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
Job Description & How to Apply Below

Medi View is building the future of surgical guidance and navigation with augmented reality and artificial intelligence. Our team is seeking a driven, skilled, and highly motivated individual for the role of Clinical Specialist. This position will be responsible for maintaining strong relationships with clinicians and onsite staff while providing support for the use of Medi View technology in interventional radiology and surgical environments while strictly adhering to all quality system and patient privacy (HIPAA) protocols.

This individual will support clinical training efforts internally and externally to customers while providing feedback regarding products and implementation to the quality, clinical, and development teams.

Essential Duties and Responsibilities Clinical Support
  • Attend cases utilizing Medi View technology, support the use of our devices for surgical navigation, and work with the commercial team to improve market share while providing high-quality service to customers. Responsible for pre-case set up, intra-operative guidance, and post-case data capture as applicable.
  • Support the use of Medi View technology during clinical trials, answer questions related to features and workflow in an intraprocedural environment.
  • Work with hospital staff and operations to forecast and manage onsite disposable inventory and ensure sites have adequate supplies for procedures and ensure proper inventory control, traceability, and segregation/return of expired or damaged product per quality system procedures.
  • Respond to customer needs and complaints regarding products and services by developing creative solutions that simplify workflow and produce scalability. Immediately identify and document all product complaints, adverse events (AEs), and potential malfunctions, reporting them to the quality team per established quality system procedures.
  • Support marketing and commercial teams for large trade shows and showcase events such as SIR, RSNA, SIO, etc.
  • Complete the required quality documentation on the usage of products in order to better understand utility and market trends including detailed procedure logs, case reports, and post-market surveillance data forms as applicable.
  • Collaborate with the commercial and sales team to support demos and sales conversations that increase market share
Clinical Training
  • Responsible for supporting the education of clinicians, proceduralists, and support staff for product installations and use ensuring all training is conducted using the current approved and controlled training materials, user manuals, and instructions for use (IFU).
  • Educate and train new employees on the use of XR90 and other products in order to provide a robust clinical understanding for non-clinical employees responsible for the development and advancement of our technology.
  • Work with the commercial and clinical affairs team to determine site-specific workflow implementation of products at customer and research sites prior to product installs for purchases, placements, evaluations, and research agreements.
Internal Training and Feedback
  • Responsible for the development, implementation, and provision of hands-on and virtual education for Medi View flagship products with internal staff.
  • Work with the project team, development, advanced development, hardware and software teams to internally disseminate regular updates and demos sharing new features that have been developed but not productized.
Communication and Meetings
  • Participate in project meetings and provide feedback regarding device use and end user workflow requirements to inform product design, risk management files, and future labeling.
Additional Responsibilities
  • Previous experience with medical devices or medical technology studies preferred
  • Previous experience with Quality Improvement Databases and Quality Management Systems preferred
  • Ability to understand basic and complex medical details
  • Knowledge of regulatory regulations and guidelines on medical devices
  • Ability to travel up to 75%

This position would report to the Director of Clinical Affairs at Medi View XR and the supervisor would define attainable goals for each quarter. This position would meet with their supervisor and the rest of the clinical team on a regular basis, while also providing autonomy and authorship of key deliverables.

  • Interpersonal communication and professional conduct within a healthcare environment.
  • Use of technology (computer, augmented reality headsets, ultrasound equipment, other imaging systems).
  • Technical writing skills for documenting procedures, non-conformance reports, and case summaries.
Qualifications

To perform this job successfully, an applicant must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Education and/or Experience – Associate or Bachelor of Science in a…
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