Senior Specialist, Clinical Education THV AR (MidWest US)

About the role

Join us and be part of our inspiring journey. You will make an impact by:

• Pre-Procedural, Intra-Procedural, Post-Procedural Case Support
• Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time guidance during clinical trial implants, including contingency planning to address unforeseen occurrences in support of assigned clinical investigations
• Education Support
• Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience
• Develop and conduct one-on-one ad hoc training sessions and in-service structured education programs
• Provide physicians and medical staff with required follow-up support to ensure continuity of education and technical support related to all aspects of clinical research
• Aid in Clinical Monitoring activities
• Ensure device accountability by tracking the location of all clinical trial devices. Manage inventory to include par levels, expiration dates, and initiate shipments and returns of investigational products according to regulatory and company guidelines
• Collaborate with product development teams to provide feedback on device iterations and new device development

Responsibilities

You will make an impact by:

• Pre-Procedural, Intra-Procedural, Post-Procedural Case Support
• Represent the Clinical Affairs Research Team during clinical trial cases with investigating physicians, hospital staff and clinical research coordinators by providing on-site, real-time guidance during clinical trial implants, including contingency planning to address unforeseen occurrences in support of assigned clinical investigations
• Education Support
• Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience
• Develop and conduct one-on-one ad hoc training sessions and in-service structured education programs
• Provide physicians and medical staff with required follow-up support to ensure continuity of education and technical support related to all aspects of clinical research
• Aid in Clinical Monitoring activities
• Ensure device accountability by tracking the location of all clinical trial devices. Manage inventory to include par levels, expiration dates, and initiate shipments and returns of investigational products according to regulatory and company guidelines
• Collaborate with product development teams to provide feedback on device iterations and new device development

Requirements

• 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%

Qualifications

• Experience in interventional cardiology, cardiothoracic surgery, 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

Skills

• Scientific curiosity and passion for evaluating data
• Passion for transforming patient care with pioneering technologies

Benefits

• Competitive salaries
• Performance-based incentives
• A wide variety of benefits programs

Pay

The base pay range for this position is $134,000 to $190,000 (highly experienced).

Schedule

Not specified.

Application Instructions

Applications will be accepted while this position is posted on our Careers website.