Clinical Specialist, Peripheral Vascular Devices

Reflow Medical, Inc.; Cincinnati (OH); On-site; USD 85,000 - 110,000; Full time

Job summary

Reflow Medical, Inc. in Cincinnati, OH seeks a Clinical Specialist to provide on-site clinical and technical support for peripheral vascular devices in both commercial and pre-commercial settings.

You will partner with the Regional Sales Director and Territory Managers to support procedural success, deliver education, and contribute to regional sales objectives while maintaining current knowledge of clinical data and regulatory requirements.

Qualifications

• RN/RT or similar accreditation is required.
• Experience in peripheral procedures is required.
• Coronary procedural experience preferred.
• Prior medical device industry experience preferred (required for Clinical Specialist II)

Responsibilities

• Provide on-site procedural coverage for Peripheral Vascular interventions.
• Deliver product education and in-service training to physicians, nurses, and technologists.
• Support safe and effective product utilization per guidelines and IFU.
• Partner with Territory Managers to support account development and sales growth.
• Develop and maintain professional relationships with healthcare providers and stakeholders.
• Communicate field insights and customer feedback to internal teams.
• Maintain knowledge of clinical data, industry trends, and regulatory requirements.
• Manage trunk stock and consignment inventory per guidelines.
• Process purchase orders per company and customer guidelines

Skills

RN/RT background

Communication skills

Relationship building

Education

Bachelor’s degree preferred

Job description

Reflow Medical, Inc. in Cincinnati, OH seeks a Clinical Specialist to provide on-site clinical and technical support for peripheral vascular devices in both commercial and pre-commercial settings.

You will partner with the Regional Sales Director and Territory Managers to support procedural success, deliver education, and contribute to regional sales objectives while maintaining current knowledge of clinical data and regulatory requirements.