Senior Specialist, Clinical Education THV AR

Edwards Lifesciences

. Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff, and clinical research coordinators .

Posted 10/13/2026full-timeRemote • United StatesSenior💰 $134,000 - $190,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial management, including on-site guidance, training, and documentation of procedural observations. Proficient in interventional cardiology and medical device regulatory requirements, with a strong focus on collaboration and education for clinical staff.

Highest-signal resume keywords

Clinical Trial ManagementInterventional Cardiology ExperienceTAVR ExperienceRegulatory Requirements KnowledgeTraining Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Intra-Operative ProceduresDevice HandlingTroubleshooting TechniquesClinical MonitoringDevice AccountabilityAdverse Events ReportingCardiovascular Science KnowledgeInventory ManagementContingency PlanningDocumentation of Case Observations

Soft Skills

CollaborationEducationCommunicationGuidanceSupport

Certifications & Qualifications

Registered Nursing Degree (RN)Radiologic Technologist (RT)Operating Room Technician (ORT)Cardiovascular Technician (RCIS)Registered Diagnostic Cardiac Sonographer (RDCS)

Industry Keywords

Clinical AffairsClinical TrialsCardiothoracic SurgeryHemodynamic Monitoring TechnologyMedical Device

About the role

Key responsibilities & impact

Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff, and clinical research coordinators
Provide on-site, real-time guidance during clinical trial implants, including contingency planning for unforeseen occurrences
Provide education on device handling, implantation, and troubleshooting techniques
Document procedural case observations for insights into post-procedural events
Develop and continuously improve training curricula, materials, and tools based on clinical trial experience
Educate and train physicians and hospital personnel on investigational products and procedures
Provide follow-up support to physicians and medical staff throughout clinical investigations
Assist in clinical monitoring activities
Track clinical trial device locations and manage inventory, par levels, expiration dates, shipments, and returns
Collaborate with product development teams to provide feedback on device iterations and new device development

Requirements

What you’ll need

Bachelor's Degree and a minimum of 5 years clinician experience in intra-operative procedures acquired from Registered Nursing Degree curriculum (RN), or in positions such as Radiologic Technologist (RT), Operating Room Technician (ORT), or Cardiovascular Technician (RCIS), or related medical device, clinical, or Certification in RDCS (Registered Diagnostic Cardiac Sonographer) within ARDMS (American Registry for Diagnostic Medical Sonography), or equivalent experience based on Edwards criteria
Ability to travel up to 75%
Experience in interventional cardiology, cardiothoracic surgery, or hemodynamic monitoring technology
Previous TAVR experience
Knowledge and understanding of cardiovascular science
Moderate understanding of medical device regulatory requirements and documents, device accountability, and adverse events reporting

Benefits

Comp & perks

Competitive salaries
Performance-based incentives
A wide variety of benefits programs to address the diverse individual needs of employees and their families