Sr. Clinical Interventional Radiology Specialist
Location
United States
Posted
9 days ago
Salary
Not specified
No structured requirement data.
Job Description
Role Description
The Sr. Clinical Interventional Radiology Specialist will collaborate with stakeholders to develop and implement innovative procedural solutions for current and future indications of the Company’s system(s). This role is pivotal in optimizing workflows, driving continuous improvement initiatives, and ensuring procedural standardization across various clinical applications.
- Lead, mentor, and develop Procedure Development Specialists and Clinical Specialists across the Company’s system(s) and indications.
- Participate in the planning, execution, and documentation of scientific and engineering experiments related to acoustic, electrical, and mechanical system components.
- Collaborate with R&D, regulatory affairs, clinical teams, and human factors to define requirements, and design outputs that align with customer and clinical needs.
- Act as a primary technical resource for the Company’s system(s) during clinical trials and feasibility studies.
- Develop and execute training programs and materials for global and domestic clinical studies.
- Participate in the execution of formative, summative, and post-market assessments to inform feature development and procedural workflows.
- Support and train internal education and clinical teams on new features, indications and continuous improvement projects (system, subsystem and software).
- Implement continuous improvement initiatives to enhance workflow efficiency and ensure best practices across indications.
Qualifications
- Bachelor’s degree in a relevant field required (e.g., Biomedical Engineering, Life Sciences, Nursing, or related discipline); advanced degree preferred.
- ARRT certification in IR required.
- 5+ years of clinical patient care experience required.
- 2+ years of experience in the medical device industry required, with direct exposure to clinical case coverage and customer support in procedural settings.
- Willing and able to travel (by automobile or air, day trips and overnight stays) up to 70% of the time both domestically and internationally.
- Proven ability to collect, synthesize, and communicate user feedback to internal teams to drive continuous product improvement.
- Demonstrated success in collaborating with cross-functional teams (R&D, marketing, clinical, regulatory, and engineering) to define new technology features and enhancements.
- Strong understanding of clinical workflows, hospital environments, and device integration in surgical or diagnostic settings.
- Excellent communication, presentation, and interpersonal skills, with the ability to engage effectively with clinicians, KOLs, and internal stakeholders.
- Ability to translate clinical needs into technical requirements and contribute to product development discussions.
- Comfortable working in a fast-paced, innovation-driven environment with multiple concurrent priorities.
- Familiarity with human factors engineering, usability studies, or post-market surveillance.
- Strong analytical mindset and ability to interpret user data, metrics, and clinical outcomes to inform development priorities.
- Demonstrated experience helping to launch or iterate new medical device technologies based on end-user feedback.
- Experience with clinical trial protocols, Good Clinical Practice (GCP), and medical device risk management is a plus.
Benefits
- Comprehensive health, dental, and vision insurance
- Life, short-term and long-term disability insurance
- 401(k)
- Paid time off
- Equal opportunity employer valuing diversity
Job Requirements
- Bachelor’s degree in a relevant field required (e.g., Biomedical Engineering, Life Sciences, Nursing, or related discipline); advanced degree preferred.
- ARRT certification in IR required.
- 5+ years of clinical patient care experience required.
- 2+ years of experience in the medical device industry required, with direct exposure to clinical case coverage and customer support in procedural settings.
- Willing and able to travel (by automobile or air, day trips and overnight stays) up to 70% of the time both domestically and internationally.
- Proven ability to collect, synthesize, and communicate user feedback to internal teams to drive continuous product improvement.
- Demonstrated success in collaborating with cross-functional teams (R&D, marketing, clinical, regulatory, and engineering) to define new technology features and enhancements.
- Strong understanding of clinical workflows, hospital environments, and device integration in surgical or diagnostic settings.
- Excellent communication, presentation, and interpersonal skills, with the ability to engage effectively with clinicians, KOLs, and internal stakeholders.
- Ability to translate clinical needs into technical requirements and contribute to product development discussions.
- Comfortable working in a fast-paced, innovation-driven environment with multiple concurrent priorities.
- Familiarity with human factors engineering, usability studies, or post-market surveillance.
- Strong analytical mindset and ability to interpret user data, metrics, and clinical outcomes to inform development priorities.
- Demonstrated experience helping to launch or iterate new medical device technologies based on end-user feedback.
- Experience with clinical trial protocols, Good Clinical Practice (GCP), and medical device risk management is a plus.
Benefits
- Comprehensive health, dental, and vision insurance
- Life, short-term and long-term disability insurance
- 401(k)
- Paid time off
- Equal opportunity employer valuing diversity
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