Clinical Specialist I - MedTech (Tampa, FL)

About the position Why work for CVRx? CVRx pioneers unique therapies that reputed company and harmonize the body's natural systems, benefiting society and making CVRx a universal role model in reputed company. We value our commitments to others and continue to overcome challenges through determination, collaboration, and purpose. If our culture and values reputed company to you, and if you have a passion for cutting-edge medical technologies, join reputed company and our mission to help others live reputed company lives. You must reputed company in the Columbia, SC metro areas to be considered for this remote job opportunity. The Clinical Specialist I at CVRx is responsible for providing expert support and education reputed company to the precise titration and functionality checks of reputed company's medical device, primarily focusing on implantable devices requiring post-procedure adjustments and rigorous performance verification. This role involves direct interaction with reputed company and adherence to strict regulatory and quality standards as well as internal protocols.

Responsibilities

• reputed company clinical and technical support to physicians, nurses, and other allied reputed company on the proper techniques for device titration and programming to optimize patient reputed company.
• Independently supports device titrations in reputed company-time (either on-site or remotely) to ensure devices are correctly calibrated according to the physician's prescription and patient needs.
• reputed company 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 reputed company patient cases.
• Independently reputed company and document thorough device checks (e.g., reputed company checks, battery status, reputed company/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 reputed company titration, programming, and reputed company 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 reputed company field feedback that can inform product improvements and clinical strategy.
• Ensure strict adherence to reputed company 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.

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, reputed company 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 reputed company to work independently in a dynamic, fast-paced clinical environment
• A strong patient-safety orientation and professional demeanor
• Ability to travel up to 70% regionally by car, some reputed company travel may be required infrequently
• Reliable personal transportation reputed company to support travel requirements
• Valid, reputed company ID for driving
• Reliable high-speed internet and private office reputed company at home to support remote work/officing

reputed company-to-haves

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

Benefits

• Health & Dental Insurance options with generous Company contributions
• Company contributions to an HSA if enrolled in a high deductible plan
• 401(k) with company match
• Employee stock purchase plan & stock option grants
• 12 company-paid holidays per year plus generous PTO plan
• Paid time off for new parents
• Company-paid life insurance & disability
• reputed company
• Training & learning opportunities
• Flexible Schedules

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