Location
Remote
Description
- Gaining an in-depth knowledge of our 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 company 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
- Clinical Studies
- Serve as a resource to investigational/research centers, as well as company 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 Management support
- Support the company 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
Requirements
- Certified Clinical Perfusionist degree strongly preferred
- Other possible degrees: Bachelor’s degree in other health profession, science, or engineering field with a strong technical and clinical background. Masters degree preferred.
- 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
- Have a full driver’s license
- Demonstrate aptitude in and knowledge of relevant therapeutic areas and ability to learn and integrate new/different therapeutic areas
- Experience in a clinical setting and clinical studies is beneficial
- Knowledge of project management tools and practices
- Proven ability to work in a matrix organization
- Ability to work independently and as a part of a team
- Have an analytic approach to problem solving
- Excellent presentation and computer skills
- Strong communicator, capable of effectively presenting ideas and concepts
- Excellent organizational skills and attention to detail
Apply
If interested contact Ashley Hipps at Ashley.Hipps@hueman.com.
Posted: Wednesday, February 18, 2026