Clinical Research Engineer – Organ Preservation & Trials

OrganOx Limited; Oklahoma; On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

401(k) match

Health, dental, vision

Paid time off

Wellness facility

Employee discounts

Job summary

OrganOx Limited in the United States seeks a Clinical Research Engineer to become a subject matter expert on OrganOx FDA approved and investigational devices, supporting clinical procedures and IDE studies.

You will train Clinical Specialists and customers, attend cases, coordinate with Development and Engineering to answer technical questions, and help build study protocols and data collection. Travel across North America is required; a perfusion/medical device background is preferred.

Qualifications

• Certified Clinical Perfusionist degree strongly preferred.
• Experience with perfusion devices and management of patients or donor organs is a must.
• Right to work in the USA.
• Be able to travel regularly within North America as required.

Responsibilities

• Gain in-depth knowledge of OrganOx FDA approved and investigational devices and clinical procedures.
• Serve as subject matter expert on devices during IDE studies and research projects.
• Support training of OrganOx employees and customers on approved, IDE and research products.
• Attend cases with investigational device as technical and clinical resource for staff.
• Interface with Development and Engineering to obtain answers to technical questions and provide feedback.

Skills

Strong communicator

Excellent presentation skills

Analytical problem solving

Organizational skills

Teamwork and independence

Education

Certified Clinical Perfusionist degree

Bachelor’s degree in health profession/science/engineering

Masters degree preferred

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

OrganOx Limited in the United States seeks a Clinical Research Engineer to become a subject matter expert on OrganOx FDA approved and investigational devices, supporting clinical procedures and IDE studies.

You will train Clinical Specialists and customers, attend cases, coordinate with Development and Engineering to answer technical questions, and help build study protocols and data collection. Travel across North America is required; a perfusion/medical device background is preferred.