General Electric Clinical Development Specialist in Little Rock, Arkansas

About Us:

GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry.

GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is an Equal Opportunity Employer at http://www.ge.com/sites/default/files/15-000845%20EEO%20combined.pdf . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Role Summary:

This position provides industry leading advanced applications support for the development of Magnetic Resonance scanners, applications and coils. The primary responsibility of this specialist is to act as clinical “voice of the customer”, ensure product solutions meet customer requirements, provide support to global program teams, and to participate in various new product introductions related activities, with a primary focus on clinical support for development of new coil technologies.

Essential Responsibilities:

Duties include (but are not limited to):

  1. Provide clinical support for the development of Magnetic Resonance Imaging products.

  2. Provide clinical support for the development of new coil technologies.

  3. Work with global engineering to develop post-processing features and new coil technologies by providing clinical input from customers.

  4. Apply knowledge of clinical MR post processing needs to guide definition and development of new imaging and post-processing techniques and new coil technologies.

  5. Evaluate performance and quality of coils and features throughout the development process by designing protocols, traveling to partner sites for installation and testing.

  6. Assist with customer complaints, investigations, offer product solutions.

  7. Develop (clinical) competitive intelligence to support the field with counter arguments and selling advantages.

  8. Support scientific congresses, customer seminars and internal training events.

  9. Ensure high quality of MR post processing training delivery to the field applications teams and sales/marketing team.

Qualifications/Requirements:

  1. Certified Radiologic Technologist (ARRT) or global equivalent.

  2. At least 5 years of experience in MR post processing, including all clinical applications and performing procedures.

  3. Ability to travel 10-20% of the time

  4. At least 5 years of experience in communicating scientific data (talks, posters, papers).

Quality Specific Goals:

  1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position.

  2. Complete all planned Quality & Compliance training within the defined deadlines.

  3. Identify and report any quality or compliance concerns and take immediate corrective action as required

Desired Characteristics:

  1. Advanced degree (Bachelors or Masters)

  2. Previous experience of clinical studies / study coordination including study documentation

  3. At least 10 yrs. experience in the medical industry

  4. Applications experience

  5. Previous GE Healthcare experience

  6. Two vacancies: 1 based in Waukesha, WI and 1 in Aurora, OH.

Locations: United States; Ohio, Wisconsin; Waukesha, Aurora

GE will only employ those who are legally authorized to work in the United States for this opening.