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Edwards Lifesciences

Senior Specialist, Clinical Education, Clinical Development

Edwards Lifesciences

. Serve as a subject matter expert supporting the advancement of transcatheter therapies through hands-on clinical engagement, procedural innovation, and continuous learning .

Posted 9/24/2026full-timeIrvine • California • United StatesSenior💰 $134,000 - $190,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in transcatheter therapies, clinical imaging, and procedural innovation, with a strong foundation in cardiovascular science and medical device regulatory requirements. Capable of providing real-time guidance during complex procedures and developing educational materials for cross-functional teams.

Highest-signal resume keywords
Transcatheter Therapies ExpertiseCardiovascular Anatomy KnowledgeClinical Imaging ProficiencyMedical Device Regulatory UnderstandingCustomer-Facing Engagement

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Procedural InnovationComplex Case SupportStatistical TechniquesDocumentation SkillsTraining DevelopmentProblem-SolvingAnalytical SkillsCritical ThinkingDevice Handling TechniquesContingency Planning
Soft Skills
Leadership SkillsInterpersonal Relationship SkillsOrganizational SkillsCommunication SkillsInfluencing Change
Tools & Technologies
Microsoft Office SuiteClinical Imaging ToolsDesign Control Documentation
Industry Keywords
Cardiovascular ScienceMedical Device ManufacturingEnvironmental Health and SafetyQuality GuidelinesAdverse Events Reporting

About the role

Key responsibilities & impact
  • Serve as a subject matter expert supporting the advancement of transcatheter therapies through hands-on clinical engagement, procedural innovation, and continuous learning
  • Partner cross-functionally with physicians, R&D, and commercial teams to support complex cases, develop procedural techniques, and translate real-world clinical insights into device and therapy improvements
  • Represent TMTT during complex research cases, clinical trials, and commercial cases with investigating physicians, hospital staff, and clinical research coordinators
  • Provide on-site, real-time guidance during implants, including contingency planning for unforeseen occurrences involving novel devices
  • Document procedural case observations and provide insights into post-procedural events
  • Support enrollment discussions and issue escalation with Principal Investigators and research teams
  • Develop materials and provide education on device handling, implantation, and troubleshooting techniques
  • Develop, analyze, and optimize complex procedures, testing, and therapies using clinical imaging knowledge
  • Coordinate clinical imaging training and instruction for cross-functional teams as products progress from ESAPCU to early human use and commercial settings
  • Create complex design control and trial-related documentation
  • Support complaint and investigational analyses and recommend improvements

Requirements

What you’ll need
  • Bachelor's Degree in Engineering or Scientific field, with 4 years experience including either industry or industry/education
  • Master's Degree or equivalent in Engineering or Scientific field, with 3 years experience including either industry or industry/education
  • Tricuspid or Mitral procedural experience within OR Cath Lab as Proctor or Industry Case Support preferred
  • Demonstrated experience in customer-facing roles, including direct engagement with physicians and leading training and procedures on procedural execution and best practices
  • Substantial knowledge and understanding of principles, theories, and concepts relevant to Engineering and cardiovascular science
  • Full knowledge of cardiovascular anatomy, pathology, and physiology
  • Strong problem-solving, organizational, analytical, and critical thinking skills
  • Substantial understanding of medical device regulatory requirements and documents, adverse events reporting
  • Good leadership skills and ability to influence change
  • Strong documentation, written and verbal communication, and interpersonal relationship skills including consultative and relationship management skills
  • Basic understanding of statistical techniques
  • Previous experience working with lab preferred
  • Knowledge of and adherence to Edwards Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing
  • Proven expertise in Microsoft Office Suite including Word, PowerPoint, Access, and Excel
  • Adherence to company rules and requirements, including pandemic protocols and Environmental Health & Safety rules
  • Ability to travel up to 50% nationwide

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