
Principal Field Clinical Specialist – Mitral & Tricuspid
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in Kansas, +1 more state.
• Provide daily clinical study support in the field, including technical assistance, education, site management, coordination, and training for Mitral and Tricuspid Therapies clinical programs.
• Advocate for clinical programs by educating investigators, introducing new technologies, and supporting cases to ensure safe patient outcomes and achieve company goals.
• Conduct on-site educational sessions and/or consulting services.
• Assist field personnel in delivering outcomes and services to Medtronic customers.
• Collaborate with cross-functional teams to formulate and implement enrollment strategies.
• Engage in conventions, forums, and meetings to enhance product awareness.
• Provide customer case support and educational resources in partnership with Therapy Development Management.
• Identify and promote growth opportunities alongside the Clinical Support Team.
• Act as a technical expert for a specific medical product or solution.
• Assist with clinical study procedures, including the preparation of the Intrepid TMVR/TTVR device and case support.
• Offer technical assistance, troubleshoot devices and systems, and support device suitability and patient selection.
• Deliver comprehensive support across echocardiography, angiography, and CT imaging modalities.
• Provide feedback from clinical sites regarding product engineering designs and improvements to support research and development efforts.
• Build and maintain relationships with customers and provide enrollment support to assigned sites.
• Establish and nurture relationships with principal investigators, research coordinators, operating room/cath lab personnel, nursing units, decision-makers, and administrative staff.
• Serve as the main contact during patient screening and enrollment, and gather necessary screening materials.
• Oversee communication regarding the shipping and return of products in accordance with Medtronic policies.
• Assist in the creation and delivery of physician training materials, simulations, benchtop models, didactic sessions, and case studies.
• Educate and train customer sites on technical issues through training sessions, in-service programs, seminars, and symposiums.
• Provide training and resources for procedure certification and activation.
• Mentor and train internal Medtronic employees.
• High school diploma with a minimum of 8 years of clinical support experience, or an Associate degree with at least 6 years, or a Bachelor’s degree with a minimum of 4 years, or an Advanced degree with at least 2 years of clinical support.
• Willingness to travel approximately 75%, including internationally.
• Capability to work in Cath Labs or Operating Rooms with potential radiation exposure.
• Ability to conduct company business outside the standard Monday through Friday, 8:00 AM to 5:00 PM work schedule.
• Must be able to lift up to 20 pounds.
• Adequate hearing, vision, and speaking abilities.
• Proficiency in using computers and CT reconstruction software.
• Ability to travel extensively by car and plane.
• Capability to sit and stand for 8 hours a day.
• Must wear a lead apron for extended periods (2-3 hours on average).
• Ability to operate a moving vehicle.
• Must adhere to all required personal protective equipment (PPE) guidelines.
• Possession of a valid driver's license and an active vehicle insurance policy; driving record will be evaluated.
• Willingness to travel with overnight stays up to 75% of the time, including internationally.
• For degrees obtained outside the United States, a degree that meets the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is necessary.
• A minimum of 3 years of experience in the Structural Heart industry field is preferred.
• Familiarity with echocardiographic imaging of the mitral and/or tricuspid valve is preferred.
• Experience with CT segmentation & analysis software, such as 3Mensio, is preferred.
• Experience with trans-septal procedures, including TMVR or LAAC or other related therapies, is preferred.
• Clinical Research experience, including coordination of multi-center trials and/or substantial structural heart field experience, is preferred.
• Experience in presenting, writing, and teaching clinical and medical information is preferred.
• Familiarity with group presentations and interventional/surgical cardiac procedures is preferred.
• Knowledge of Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials is preferred.
• Proficiency in MS Office applications: Excel, PowerPoint, Word, MS Project or similar scheduling software, and project management techniques and tools is preferred.
• U.S. work authorization is required; sponsorship is available for Principal-level roles and above.
• Competitive Salary and flexible Benefits Package.
• Health, Dental, and Vision insurance.
• Health Savings Account.
• Healthcare Flexible Spending Account.
• Life insurance.
• Long-term disability leave.
• Dependent daycare spending account.
• Tuition assistance/reimbursement.
• Simple Steps (global well-being program).
• Incentive plans.
• 401(k) plan with employer contribution and matching.
• Short-term disability.
• Paid time off.
• Paid holidays.
• Employee Stock Purchase Plan.
• Employee Assistance Program.
• Non-qualified Retirement Plan Supplement.
• Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
• Paid sick time, as mandated by applicable state law, for temporary employees.
• Reasonable accommodations for qualified individuals with disabilities.
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