Clinical Specialist I - MedTech (Tampa, FL)

CVRx, Inc.•Tampa, FL

1d•Remote

About The Position

CVRx pioneers unique therapies that harness and harmonize the body's natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration, and purpose. If our culture and values speak to you, and if you have a passion for cutting-edge medical technologies, join our team and our mission to help others live better lives. The Clinical Specialist at CVRx is responsible for providing expert support and education related to the precise titration and functionality checks of our company's medical device, primarily focusing on implantable devices requiring post-procedure adjustments and rigorous performance verification. This role involves direct interaction with healthcare professionals and adherence to strict regulatory and quality standards as well as internal protocols.

Requirements

Bachelor's degree in a relevant scientific or technical field (e.g., Biomedical Engineering, Nursing, Cardiovascular Technology, or equivalent experience)
Exceptional understanding of medical terminology, human anatomy, and disease states relevant to the device technology
Strong technical aptitude for operating proprietary device programming software and diagnostic equipment
Excellent written and verbal communication, presentation, and interpersonal skills
Detail-oriented with a strong commitment to quality and regulatory compliance
Self-motivated and able to work independently in a dynamic, fast-paced clinical environment
A strong patient-safety orientation and professional demeanor.
Ability to sit, stand, and walk for extended periods
Must be able to lift up to 25lbs.
Ability to travel 60% or more, some overnights may be required.
May be required to be fully vaccinated against the COVID-19 virus and other diseases.

Nice To Haves

An advanced degree is preferred
Preferred, not required experience in device programming, titration, and/or performance analysis.

Responsibilities

Provide clinical and technical support to physicians, nurses, and other allied healthcare professionals on the proper techniques for device titration and programming to optimize patient outcomes.
Assist in real-time titration procedures (either on-site or remotely) to ensure devices are correctly calibrated according to the physician's prescription and patient needs.
Educate clinical staff on advanced programming features, troubleshooting, and best practices for chronic management of the device settings.
Serve as a primary technical resource for clinical inquiries regarding device operation, troubleshooting, and complex patient cases.
Perform and document thorough device checks (e.g., integrity checks, battery status, lead/sensor impedance, therapeutic output) following implant, during follow-up, and as required by protocols.
Identify, document and report any potential device anomalies or performance deviations to the appropriate internal teams (e.g., R&D, Quality, Regulatory).
Maintain meticulous records of all titration, programming, and check procedures in compliance with company policy and regulatory requirements (e.g., FDA, ISO).
Collaborate closely with Sales, Research & Development, Clinical Affairs, and Quality teams to provide field feedback that can inform product improvements and clinical strategy.
Ensure strict adherence to all relevant regulatory guidelines (e.g., HIPAA, GDPR, medical device regulations) and company Standard Operating Procedures (SOPs).
Participate in clinical trials or post-market surveillance activities as needed, performing scheduled device checks and data collection.