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Field Clinical Specialist TAVI (Puerto Rico)

edwards

New
Mid 🇬🇧 English
MS Office

Job description

About the role

Edwards Lifesciences, whose THV business unit partners with cardiologists and clinical teams on transcatheter aortic heart valve replacement (TAVR), is looking for a Field Clinical Specialist TAVI based in Puerto Rico. The role supports clinical investigations, trains physicians and hospital staff, and works with sales on account growth.

Key responsibilities

  • Develop clinical education materials for clinical investigations and provide expertise on the device, procedure and protocol throughout the investigation lifecycle.
  • Certify centers, physicians, related staff and EW personnel according to EW SOPs, and interact with KOLs and proctors.
  • Train physicians, hospital personnel and staff on device handling, implantation and troubleshooting, and run ad hoc and in-service education programs.
  • Provide follow-up support during commercial procedures so that education and technical support continue.
  • Plan and implement growth strategies in focused accounts with Sales and Sales Management, and support upselling in key strategic accounts with Business Managers.
  • Validate software and hardware updates in the field, and review clinical support activities, market changes, assigned accounts and competitor activity with the NSM and the Sales Specialist.

Required profile

  • 3 years of previous related medical device and/or clinical experience.
  • Bachelor's degree in a related field.
  • Preferred: training experience in a clinical or technical environment.
  • Bilingual Spanish and English.
  • COVID-19 vaccination required for patient-facing and in-hospital roles, unless a medical or religious accommodation is granted.

Required skills

  • Proven expertise in MS Office Suite and ability to operate general office machinery.
  • Good written and verbal communication, presentation and negotiation skills.
  • Moderate knowledge of cardiovascular science, anatomy, pathology and physiology, and of medical device regulatory requirements and adverse event reporting.
  • Ability to manage confidential information, competing priorities and to work in teams across departments.

Questions fréquentes

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Source : ats:workday

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Published 7 hours ago

Expires 1 month from now

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