Senior Medical Device Specialist

2 days ago

Perth, Western Australia beBeeClinical Full time $140,000 - $160,000
Senior Clinical Engineer Role in Medtech

As a key member of our team, you will be responsible for supporting clinical trials across Australia. This involves providing on-site technical support during human studies, including device setup, calibration, and overnight monitoring sessions at trial sites.

You will work closely with the engineering and product teams to share field-based insights and usability feedback. Additionally, you will assist in proof-of-concept validation and mechanism-of-action verification, and document and report technical observations from the field to drive design iterations.

To excel in this role, you will need strong interpersonal and communication skills, as well as the ability to work independently under high-travel and high-pressure conditions. A tertiary qualification in Biomedical Engineering, Clinical Engineering, Science, or similar technical or business field is also required.

Preferred qualifications include previous involvement in human clinical trials, experience supporting CRO-led studies, familiarity with anatomical systems, Operating Theatre environments, or physiological monitoring technologies, and a background in EP, CRM, Neuromodulation, or other Class III devices.

Key Responsibilities:
  • Clinical Study Support: Provide on-site technical support during human studies, including device setup, calibration, and overnight monitoring sessions at trial sites.
  • Coordinate logistics and technical execution across multiple Australian study locations.
  • Support study start-up tasks, including site qualification, equipment delivery, and protocol compliance.
  • Collaborate with CROs, clinical teams, and local investigators to ensure protocol fidelity and data quality.
Technical Development & Feedback:
  • Interface with engineering and product teams to share field-based insights and usability feedback.
  • Work with complex equipment configurations, including third-party systems.
  • Assist in proof-of-concept validation and mechanism-of-action verification.
  • Document and report technical observations from the field to drive design iterations.
Training & Documentation:
  • Deliver hands-on and classroom-style training to site personnel on study procedures and device usage.
  • Support the development of training materials and standard operating procedures.
  • Review study documentation, such as protocols and technical manuals, and contribute to site readiness.
Qualifications & Experience:
  • Tertiary qualification in Biomedical Engineering, Clinical Engineering, Science, or similar technical or business field.
  • Proven experience in a hands-on clinical, technical support, or device-focused role.
  • Strong interpersonal and communication skills.
  • Minimum 2+ years commercial or Clinical Research Trial experience.
  • Ability to work independently under high-travel and high-pressure conditions.
Preferred Qualifications:
  • Previous involvement in human clinical trials and/or experience supporting CRO-led studies.
  • Familiarity with anatomical systems, Operating Theatre environments, or physiological monitoring technologies.
  • Background in EP, CRM, Neuromodulation, or other Class III devices.

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