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OrganOxPosted 30+ days ago

Clinical Research Engineer

Full-time
Remote
Mid level
Competitive
Posted 30+ days ago

OrganOx is a commercial-stage organ technology company developing technologies to improve outcomes for patients with acute or chronic organ failure. The Clinical Research Engineer serves as a subject matter expert on OrganOx devices and associated clinical procedures, supports training, and contributes to clinical studies, data collection, regulatory submissions, and clinical operations.

Posted
30+ Days Ago
Source
apply.workable.com
Sector
Healthcare

Opens the employer's application page in a new tab

Responsibilities

  • Gaining an in-depth knowledge of OrganOx FDA approved and investigational or research products, as well as associated clinical procedures
  • Serving as the subject matter expert on the device and procedures during IDE studies and research projects
  • Supporting training of OrganOx employees (e.g. Clinical Specialists) and customers on OrganOx approved, as well as IDE and research products and studies
  • Gaining an in-depth knowledge of OrganOx FDA approved and investigational/research products, as well as associated clinical procedures
  • Support the development of training and other support materials for FDA approved and investigational/research devices and procedures
  • Train investigational/research centers, Clinical Specialists, and other OrganOx personnel on investigational/research devices and procedures
  • Attend cases with investigational/research device as a technical and clinical resource for the staff at the investigational/research center
  • Interface with Development and Engineering in order to obtain answers to technical questions
  • Provide clinical and technical feedback on FDA approved and investigational/research device to Development and Engineering
  • Serve as a resource to investigational/research centers, as well as OrganOx personnel, regarding investigational/research devices and clinical study protocols
  • Support the development of clinical study protocols
  • Support sound and thorough data collection ensure data analysis in accordance with the protocol
  • Develop training and other support materials for clinical protocols, study procedures, data collection and review
  • Assist in the development and implementation of a study-specific database for clinical studies
  • Assist Clinical Research Associates with review of study data
  • Support writing and review of clinical study reports and the clinical portion of FDA submissions
  • Identify and report study protocol challenges and compliance issues to clinical management
  • Support OrganOx in maintaining current and developing professional relationships with investigators and investigational/research sites
  • Serve as a resource to clinical management for departmental decisions related to continuing quality improvement of process and procedures
  • Other duties as assigned by VP, Clinical Affairs & Training

Qualifications

  • Other possible degrees: Bachelor's degree in other health profession, science, or engineering field with a strong technical and clinical background
  • Experience with perfusion devices and management of patients or donor organs is a must
  • Previous experience in the medical device industry with preference for transplant and perfusion devices is desired
  • Computer literate and familiar with Word, Excel, and PowerPoint
  • Be able to travel regularly within North America as required
  • Right to work in the USA
  • Have a full driver's license

Preferred

  • Certified Clinical Perfusionist degree strongly preferred
  • Masters degree preferred
  • Master’s degree

Required skills

Perfusion DevicesClinical StudiesMedical Device IndustryMicrosoft WordMicrosoft ExcelMicrosoft PowerPoint

Nice to have

Masters degree preferred

Full job description

OrganOx is a commercial-stage organ technology company developing technologies to improve outcomes for patients with acute or chronic organ failure. The Clinical Research Engineer serves as a subject matter expert on OrganOx devices and associated clinical procedures, supports training, and contributes to clinical studies, data collection, regulatory submissions, and clinical operations.

Responsibilities

  • Gaining an in-depth knowledge of OrganOx FDA approved and investigational or research products, as well as associated clinical procedures
  • Serving as the subject matter expert on the device and procedures during IDE studies and research projects
  • Supporting training of OrganOx employees (e.g. Clinical Specialists) and customers on OrganOx approved, as well as IDE and research products and studies
  • Gaining an in-depth knowledge of OrganOx FDA approved and investigational/research products, as well as associated clinical procedures
  • Support the development of training and other support materials for FDA approved and investigational/research devices and procedures
  • Train investigational/research centers, Clinical Specialists, and other OrganOx personnel on investigational/research devices and procedures
  • Attend cases with investigational/research device as a technical and clinical resource for the staff at the investigational/research center
  • Interface with Development and Engineering in order to obtain answers to technical questions
  • Provide clinical and technical feedback on FDA approved and investigational/research device to Development and Engineering
  • Serve as a resource to investigational/research centers, as well as OrganOx personnel, regarding investigational/research devices and clinical study protocols
  • Support the development of clinical study protocols
  • Support sound and thorough data collection ensure data analysis in accordance with the protocol
  • Develop training and other support materials for clinical protocols, study procedures, data collection and review
  • Assist in the development and implementation of a study-specific database for clinical studies
  • Assist Clinical Research Associates with review of study data
  • Support writing and review of clinical study reports and the clinical portion of FDA submissions
  • Identify and report study protocol challenges and compliance issues to clinical management
  • Support OrganOx in maintaining current and developing professional relationships with investigators and investigational/research sites
  • Serve as a resource to clinical management for departmental decisions related to continuing quality improvement of process and procedures
  • Other duties as assigned by VP, Clinical Affairs & Training

Preferred

  • Certified Clinical Perfusionist degree strongly preferred
  • Masters degree preferred
  • Certified Clinical Perfusionist
  • Master’s degree

Benefits

  • Health coverage available from day one
  • Dental coverage available from day one
  • Vision coverage available from day one
  • Disability coverage available from day one
  • Flexible spending accounts available from day one
  • 401(k) retirement plan with company matching after 90 days
  • Paid time off
  • Paid holidays
  • Additional leave benefits
  • Employee discounts
  • Access to an onsite wellness facility
  • Opportunities for ongoing professional development
  • Remote work arrangement

Company

  • Transportable automated liver perfusion devices for transplantation
  • Oxford, Oxfordshire, GBR
  • http://www.organox.com/
  • Founded in 2008
  • 51-200 employees

Qualifications

  • Other possible degrees: Bachelor's degree in other health profession, science, or engineering field with a strong technical and clinical background
  • Experience with perfusion devices and management of patients or donor organs is a must
  • Previous experience in the medical device industry with preference for transplant and perfusion devices is desired
  • Computer literate and familiar with Word, Excel, and PowerPoint
  • Be able to travel regularly within North America as required
  • Right to work in the USA
  • Have a full driver's license
  • Certified Clinical Perfusionist degree strongly preferred
  • Masters degree preferred

Required skills

  • Perfusion Devices, Patient and Donor Organ Management, Clinical Studies, Medical Device Industry, Microsoft Word, Microsoft Excel, Microsoft PowerPoint

Preferred skills

  • Certified Clinical Perfusionist degree strongly preferred, Masters degree preferred

Experience

  • Mid level

Job details

Employment type

Full-time

Seniority level

Mid level

Date posted

Sep 18, 2026

Work mode

Remote

Job source

apply.workable.com

Company

OrganOx

Healthcare

Transportable automated liver perfusion devices for transplantation

See all 2 jobs from OrganOx →
  • Remote, USA
  • Healthcare
  • 51-200 employees
  • Founded 2008
  • organox.com

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