Field Clinical Engineer

Do you have medical device experience? Are you interested in neuromodulation?

Neuspera Medical is looking for a contract Field Clinical Engineer for the WEST COAST.

SNAPSHOT

Base Pay : $150.00 hourly

Employment Type : Contract / Consulting

Job Type : Clinical

Education : 4 Year Engineering or Life Science Degree (preferably M.S. Engineering)

Experience : 12 years

Manages Others : No

Industry : Medical Devices

Required Travel : Up to 70% - must live on WEST COAST with easy airport access

Location : Remote or hybrid

About Neuspera Medical, Inc.

Neuspera Medical, Inc. is an exciting early-stage medical device company with a uniquely positioned neuromodulation technology platform, headquartered in San Jose, CA.

Neuspera is committed to developing implantable medical device technology that will improve the lives of patients battling chronic illness. With the first intended indication for use as Urinary Urgency Incontinence (UUI), the platform technology is ultimately designed to deliver targeted bioelectronic medicine for a variety of conditions. Neuspera's minimally invasive implants with external wearable transmitters offer the possibility for therapies to reach deeper, harder to access anatomical locations in the body.

WHY NEUSPERA?

Take the next step in your career and join Neuspera today to change lives through the products we help create. Here, you will contribute your talents to meaningful projects that impact the lives of patients around the world and develop as an individual by working directly with a team of seasoned experts and rising stars. Our values of accountability, respect, tenacity, results, and integrity are embedded in everything we do. No matter what your role may be, Neuspera strives to ensure all our employees are empowered and given the necessary tools to lead us in our relentless pursuit of success.

PRIMARY FUNCTION

Neuspera Medical is seeking a contract Field Clinical Engineer with experience supporting and managing medical device trials at research sites. The qualified consultant will be responsible for clinical trial execution and site management. This will be done by developing and leveraging positive relationships with clinical site personnel including physicians, nurses, and clinical research specialists. Duties include site selection, protocol, and product training, implant support, follow-up support, and site management. The goals of this position are to drive patient recruitment, ensure protocol and data compliance, and provide technical support for clinical procedures.

JOB DUTIES

Conduct Field Clinical Research

• Support site selection and activation process
• Deliver protocol, product, and procedure training at sites
• Provide technical implant and follow-up procedure support
• Ensure protocol compliance and data collection integrity
• Manage site performance against enrollment and data quality targets
• Serve as a liaison between company and physician investigators
• Collaborate on publications

Support Research and Development

The ideal consultant will have experience in all the above areas with an implantable medical device application background, and be familiar with working in hospitals and clinics. External relationships include physicians, clinic staff, hospital staff, and research subjects.

JOB REQUIREMENTS

Qualifications and Experience :

12 years experience, or Master's degree in Engineering or Medical Science

12 years of experience

Compensation :

$150.00 hourly contract / consulting

Work Environment :