Clinical Applications Specialist
Posted Date: 10/16/2020
Location: Remote USA
Part Time/Full Time Status: Full Time
Position Title: Clinical Application Specialist
Employee Reports To: CTO
Employee Classification: Exempt, Full-Time
Job Purpose and Summary
Centerline Biomedical, Inc., a medical device start-up with high growth potential, seeks to hire a Clinical Application Specialist. This individual would work among a diverse team of experts, itself, part of a highly-skilled multidisciplinary team dedicated to achieving the successful commercial launch of a medical device and development of next-generation technologies.
Clinical Application Specialist will provide expert clinical product, technical assistance and training to physicians and staff on the effective use of Centerline Biomedical products during interventional procedures to help drive the adoption of the IOPS System. The position reports to CTO of Centerline Biomedical Inc.
Centerline Biomedical, a Cleveland Clinic spinoff housed in the Global Cardiovascular Innovation Center (GCIC) on Cleveland Clinic’s main campus in Cleveland, Ohio, maintains a close relationship with Cleveland Clinic and has access to the unique resources and environment of the incubator to carry out research and product development with Cleveland Clinic researchers and clinicians. More information can be found on our homepage.
Core values are integral to our work at Centerline and must align with any potential candidate, those being Integrity, Accountability, Passion, Service and Development (of people)
Essential Duties and Responsibilities
- Drive adoption and usage of the IOPS at the installed hospital sites by providing continuous training, case support and ongoing presence. Provides clinical training and education to customers. Assists in disseminating technical product information to customers. Assists in the development and execution of regional hospital staff training courses.
- Coach existing IOPS users to further increase their IOPS usage skills.
- Broaden user base at each site adding and training new physician/clinician users of the IOPS system
- Serve as the first line of service (as needed) to current and future customers. Have a technical understanding of the product and the ability to troubleshoot any product technical challenges
- Process and monitor product complaint per company procedures
- Assists in advancing revenue and market position consistent with Company goals. Achieves deep and thorough account penetration and assist in developing new target accounts
Qualifications, Education and Experience
- Bachelor’s degree or equivalent training and/or experience
- At least 3 years of experience in a clinical Cath Lab or Operating Room environment
- Experience with Multi-modality Fusion Overlay
- 3D Imaging Reconstruction
- Support and/or understanding of Complex Aortic Procedures. (Nice to have)
- Ability to work in radiation field wearing necessary lead protection garments
- Ability to communicate effectively, both orally and in writing
- Ability to establish and maintain cooperative working relationships with persons contacted in the course of performing assigned duties
- Ability to maintain confidentiality as well as ability to exercise independent judgment consistent with company guidelines
- Ability to travel 75% of the time required
The general workplace policies and procedures apply to the Quality Regulatory Affairs Manager, and this position is employed as an at-will full time employee. This position may be required to work evening or weekend hours. Some degree of flexibility in core working hours is provided, as long as objectives and expectations are being met for this role.
This job description is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed within this job. However, this job description is not intended to be an exhaustive list of responsibilities, duties, or qualifications associated with the position and may be modified from time-to-time.