Sr. Tech Clinical Consultant - Cardiology

Fujifilm

103d

About The Position

The Senior Technical Clinical Consultant, Cardiology shall be responsible for all aspects of the reporting design and build, configuration, workflow, measurement/data mapping for project and or post go-live support cases in compliance with the company’s quality procedures.

Requirements

• Bachelor's degree in biomedical engineering, healthcare, computer science or registered nurse, sonographer, technologist – desired, but not required.
• 2+ years’ experience with PACS systems and configurations.
• Self-directed with excellent management skills.
• Strong interpersonal, team building and leadership skills.
• Inquisitive and creative with good decision-making skills.
• Resourceful and thorough with a strong sense of urgency.
• Strong verbal and written communication skills; professional presence.
• Ability to work effectively with customers in the medical field.
• Ability to prioritize and handle multiple functions.
• Experience in related a discipline is a plus.
• Exposure to the medical field, particularly cardiology, is a plus.

Responsibilities

• Serve as a departmental and company authority resource for all aspects of cardiology reporting.
• Participate effectively and actively in assigned implementation and post go-live support project team activities, as directed by the applicable Project and CV Clinical Support Managers.
• Consult with customers and project team members regarding existing and projected clinical workflows, Synapse Cardiology applications, best practices, and proper management of sensitive clinical data.
• Direct interaction with customers to identify applicable specifications and provide support.
• Configure, tailor, and deliver reporting application solutions in the context of a commercial project implementation.
• Configure and validate clinical measurement/data import/export interfaces.
• Design, customization, and electronic delivery of technical clinical tools and supplements.
• Compliance with respect to all applicable requirements of the company’s quality management system.
• All other functions and/or responsibilities that may be assigned by upper-level management.
• Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations and standards.
• Comply with and pass all requirements for vendor credentialing as part of gaining access to hospitals and facilities to perform assigned job duties.

Benefits

• Dynamic, flexible work environment.
• Opportunity to innovate and collaborate.

What This Job Offers

• Career Level: Mid Level
• Education Level: Bachelor's degree
• Number of Employees: 501-1,000 employees