Field Clinical Representative - Newark, NJ
Location
United States
Posted
7 days ago
Salary
$100K - $130K / year
Seniority
Mid Level
No structured requirement data.
Job Description
ABOUT INSPIRE MEDICAL SYSTEMS
Inspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive Sleep Apnea (OSA). We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Inspire Medical Systems is committed to enhancing patients’ lives through sleep innovation. We are steadfast in our commitment to prioritize patient outcomes, act with integrity and lead with respect. With positive persistence at our core, we are committed to all those we serve.
WHY JOIN OUR FAST-GROWING TEAM
At Inspire, we value people – your diverse experiences, backgrounds, and thoughts. We elevate voices and encourage learning opportunities to build a professional network that grows into community. We embrace a people-first culture by offering excellent benefits, 401k matching, ESPP, flexible time off (FTO), and tuition reimbursement.
If you’re passionate about making a difference in people’s lives and want to work with innovative technology, come be a part of our great team!
ESSENTIAL JOB FUNCTIONS
The Field Clinical Representative provides technical and clinical expertise, educational and field support to ensure the safe adoption of the Inspire therapy and products. The FCR is responsible for working with customers, physicians, clinic staff and Inspire field staff to drive procedural and practice success. #LI-Remote
OPPORTUNITIES YOU WILL HAVE IN THIS ROLE
- Provide technical support during implant procedures and at device activation.
- Maintain credentials enabling access to assigned hospitals and clinics.
- Provide technical leadership and education in assigned region to account clinical staff.
- Provide post-training follow up including procedural reviews, in servicing and support.
- Assist customers in device troubleshooting.
- Collaborate with sales personnel on appropriate training/support for targeted customers.
- Proactively disseminate peer-reviewed scientific and clinical information to customers and assigned sales team as needed.
- Provide technical expertise for assigned regional education and training activities.
- Stay current on relevant scientific publications and clinical evidence.
WHAT YOU CAN BRING TO OUR GREAT TEAM
Required:
- Bachelors’ degree and 2+ years of related clinical, healthcare or medical device industry experience (OR) Bachelor's degree and 1+ years applicable Inspire experience (OR) an Associates’ degree or Professional Certification and 5+ years of related clinical/healthcare or medical device industry experience.
- Ability to communicate and collaborate effectively in a clinical setting.
- Strong computer skills with MS office including PowerPoint and Excel.
- Problem solving/trouble shooting skills.
- Ability to travel (including overnights as needed) within territory.
Preferred:
- Degree in Nursing, Engineering, Science or technical discipline.
- Previous Operating Room (surgical) coverage with implantable devices.
#LI-Remote
The salary for this position will be offered at a level consistent with the experience and qualifications of the candidate. This information reflects the anticipated salary range for this position at the time of posting. The salary range may be modified in the future and actual compensation may vary from the posting based on various factors such as geographic location, work experience, education and/or skill level.
BENEFITS AND OTHER COMPENSATION
Inspire offers a highly competitive benefits package including (general description of the benefits and other compensation offered):
- Multiple health insurance plan options.
- Employer contributions to Health Savings Account.
- Dental, Vision, Life and Disability benefits.
- 401k plan + employer match.
- Identity Protection.
- Flexible time off.
- Tuition Reimbursement.
- Employee Assistance program.
- All employees have the opportunity to participate in the ownership and success of Inspire. Employees at all levels can participate through equity awards and the Employee Stock Purchase Program.
Inspire Medical Systems provides equal employment opportunity (EEO) to all employees and applicants without regard to race, color, religion, creed, sex, national origin, age, disability, marital status, familial status, sexual orientation, status regarding public assistance, membership or activity in a local commission, military or veteran status, genetic information, pregnancy or childbirth, or any other status protected by applicable federal, state, and local laws. This policy applies to all aspects of the employment relationship, including recruitment, hiring, compensation, promotion, transfer, disciplinary action, layoff, return from layoff, training, and social and recreational programs. Inspire Medical Systems complies with applicable laws governing non-discrimination in employment in every location in which Inspire Medical Systems has facilities. All such employment decisions will be made without unlawfully discriminating on any prohibited basis.
Inspire Medical Systems is an equal opportunity employer with recruitment efforts focused on ensuring a diverse workforce. Applicants with a disability that need accommodation to complete the Inspire Medical Systems application process should contact Human Resources at 844-672-4357 or email careers@inspiresleep(dot)com
Inspire Medical Systems participates in E-Verify.
Related Guides
Related Categories
Related Job Pages
More Clinical Research Jobs
Clinical Review Coordinator
AmeritaAmerita, an affiliate of BrightSpring Health Services, is a specialty infusion company focused on providing complex pharmaceutical products and clinical services to patients outside of the hospital. Committed to excellent service, our vision is to combine the administrative efficiencies of a large organization with the flexibility, responsiveness, and entrepreneurial spirit of a local provider.
The Clinical Review Coordinator supports patient onboarding by gathering missing information required to initiate care, working within the Clinical Review team to process new referrals efficiently. This role involves reviewing referral documents, updating patient demographics, and coordinating with pharmacists to ensure all necessary details are obtained from various sources.
Strategic Clinical Quality Manager - South Florida
Fresenius Medical CareCreating a future worth living. For patients. Worldwide. Every day.
The Clinical Quality Manager develops, implements, and monitors Quality Assurance and Performance Improvement (QAPI) programs to ensure high standards of patient care and regulatory adherence across assigned treatment modalities. This role involves leading quality initiatives, conducting audits, facilitating staff education, and collaborating with interdisciplinary teams to drive continuous improvement in patient safety and clinical quality performance.
Senior Mapping Specialist, CAS - South Carolina
MedtronicMedtronic is a global leader in medical technology, dedicated to improving healthcare through innovative therapies and devices. Known for transforming patient c
The specialist will provide clinical and technical support and training to physicians and staff on EP mapping and navigation systems and all CAS products, while promoting the safe and effective use of Company CAS products and related procedures. This role also involves understanding and supporting sales objectives to achieve or exceed sales goals within all CAS products through cultivating customer relationships.
Clinical Research Associate Manager---Regulatory
Mass General BrighamMass General Brigham connects a full spectrum of care across a system of academic medical centers, specialty and community hospitals, physician networks, a heal
The Associate Manager provides first-line supervision to research staff, overseeing daily operations and managing staff productivity and quality of work across multiple specialties. Regulatory responsibilities include maintaining study binders, preparing and submitting amendments and safety reports to the IRB, and managing adverse event documentation.
