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Field Clinical Engineer Jobs in California (NOW HIRING)

Jj

Sr Field Clinical Research Specialist

Agoura Hills, CA · On-site

$83K - $90K/yr

Bachelor's degree in engineering, nursing, biological sciences, a related field, or equivalent cardiology certification. * 6-8 years of relevant experience, including 5 years of clinical field-based ...

6326-V-Wave Inc. Legal Entity

$117 - $201/hr

Bachelor's degree in engineering, nursing, biological sciences, a related field, or equivalent cardiology certification. * 6-8 years of relevant experience, including 5years of clinical field‑based ...

New

Absolut

Clinical R&D Engineer

Los Angeles, CA · On-site

Role: Clinical R&D Engineer Duration: 6+ Months Location: Target LA, California or St Paul ... Works with field and medical personnel to define the benchmarks for evaluating the clinical ...

New

Socket.dev

Sr. Clinical Development Engineer

Sunnyvale, CA · On-site

$180 - $240/hr

Support product launches and/or clinical trials and collect early field feedback * Design Control ... Masters or PhD in Mechanical Engineering, Controls Engineering, Biomedical Engineering or similar

New

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All JobsField Clinical Engineer JobsField Clinical Engineer Jobs in California

Field Clinical Engineer information

See California salary details

$15

$33

$53

How much do field clinical engineer jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for field clinical engineer in California is $33.65, according to ZipRecruiter salary data. Most workers in this role earn between $23.70 and $40.34 per hour, depending on experience, location, and employer.

What is a field clinical engineer?

A Field Clinical Engineer (FCE) is a professional who works in the medical device industry, providing technical and clinical support for products used in healthcare settings, such as hospitals or clinics. They assist physicians and other clinicians during procedures, help with device installation and troubleshooting, and educate staff on the correct use of medical equipment. FCEs act as a bridge between the medical device company and healthcare providers, ensuring devices are used safely and effectively. Their role often involves traveling to different clinical sites, supporting product launches, and gathering feedback for product improvement.

What are the key skills and qualifications needed to thrive as a field clinical engineer?

To thrive as a Field Clinical Engineer, you need a solid background in biomedical engineering or a related field, along with in-depth knowledge of medical devices and clinical procedures. Familiarity with medical device programming, troubleshooting equipment, and relevant certifications such as CBET or manufacturer-specific training are typically required. Excellent interpersonal skills, problem-solving abilities, and the capacity to educate and support clinical staff distinguish top performers in this role. These skills are crucial for ensuring safe and effective device usage, fostering strong client relationships, and resolving technical issues in high-stakes clinical environments.

What are some common challenges faced by field clinical engineers when supporting medical device implementations?

Field Clinical Engineers often encounter challenges such as adapting quickly to different hospital protocols, communicating complex technical information to clinical staff, and troubleshooting device issues in real-time during procedures. The role requires balancing technical expertise with strong interpersonal skills to build trust with healthcare professionals. Additionally, frequent travel and irregular hours can be expected, especially when supporting urgent cases or multiple sites. Being proactive, adaptable, and maintaining up-to-date training are key to overcoming these challenges and ensuring successful device implementation.

What is the difference between Field Clinical Engineer vs Biomedical Equipment Technician?

AspectField Clinical EngineerBiomedical Equipment Technician
CredentialsBachelor's degree in engineering or related field; certifications like CBET or CCEAssociate's or bachelor's degree in biomedical technology; certifications like CBET
Work EnvironmentHospitals, medical device companies, clinical settingsHospitals, clinics, repair shops
Job FocusClinical application, device integration, troubleshooting, trainingMaintenance, repair, calibration of medical equipment
Industry UsageUsed by medical device manufacturers and healthcare providersPrimarily in healthcare facilities and service companies

While both roles involve working with medical equipment, Field Clinical Engineers focus on clinical application, device integration, and training, whereas Biomedical Equipment Technicians primarily handle maintenance and repairs. The roles often overlap but differ in scope and responsibilities within healthcare technology support.

What are popular job titles related to Field Clinical Engineer jobs in California?

For Field Clinical Engineer jobs in California, the most frequently searched job titles are:

What job categories do people searching Field Clinical Engineer jobs in California look for?

The top searched job categories for Field Clinical Engineer jobs in California are:

Field Clinical Engineer jobs near you
Infographic showing various Field Clinical Engineer job openings in California as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 12% Part Time, and 2% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $69,982 per year, or $33.6 per hour.

Sr. Clinical Research Associate

Medasource

Los Angeles, CA • On-site

$96 - $103/hr

Other

Posted 22 days ago

Job description

Sr. Field Clinical Research Associate
Remote with Travel required in the North Central Region (ideally based out of Boston, MA or Philadelphia, PA)
Hybrid role
Compensation: $70 - $75 per hour

ABOUT THE ROLE

Our client, a leading life sciences company, is seeking a Sr. Field Clinical Research Associate for a remote, travel-based, part-time 12-month contract position focused on the North Central Region, with the possibility of extension. In this hybrid role, you will be responsible for monitoring clinical studies at assigned sites to ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols. You will play a key role in site initiation, periodic and close-out visits, data and documentation review, adverse event and protocol deviation reporting, and resolution of site issues. The position involves close coordination with study teams, enrolling sites and subjects, facilitating data query resolution, and mentoring junior team members. This is an excellent opportunity for an experienced clinical research professional with a strong background in cardiac, vascular, or neuromodulation technologies.

WHAT YOU'LL DO
  • Monitor clinical studies at sites in your assigned territory (and others as requested) to ensure compliance with regulatory requirements, Good Clinical Practice, and study protocols, including site initiation, periodic, and close-out visits.
  • Ensure both regulatory and clinical protocol compliance is maintained for all assigned clinical projects.
  • Review data and source documentation from investigational sites for accuracy and completeness.
  • Ensure timely and accurate reporting of adverse events, protocol deviations, device complaints, and malfunctions according to company policies and procedures.
  • Resolve and/or facilitate resolution of site issues, including identification of root causes and actions to prevent recurrence.
  • Coordinate with study teams, field clinical engineers, and specialists to enroll sites into new and ongoing clinical studies.
  • Facilitate enrollment of study subjects via site coordinators and support resolution of data queries and action items at clinical sites.
  • Promptly report findings of monitoring visits according to established processes.
  • Collaborate with in-house teams to ensure complete and timely submission of study documents.
  • Participate in conference calls and training sessions as required.
  • Train site personnel to ensure compliance with study protocols and local regulations.
  • Mentor less experienced clinical team members as requested.
  • Demonstrate a high level of written and verbal communication skills with internal and external customers.
WHAT YOU BRING
  • Bachelor's degree from an accredited university or college, preferably in natural science, pre-medicine, nursing, bioengineering, or a related field.
  • Minimum five years of clinical research experience with a superb understanding of all aspects of clinical research.
  • Strong written, verbal, interpersonal, presentation, analytical, and organizational skills.
  • Ability to interpret basic clinical data, meet deadlines, and communicate effectively with all levels of employees.
  • Proficiency with word processing software and relevant clinical applications.
  • Ability to work independently and within a dynamic, global team environment.
  • Ability to exchange straightforward information, ask questions, and check for understanding.
  • Familiarity with cardiac, vascular, and/or neuromodulation technologies.
  • Prior clinical monitoring experience (strongly preferred).
  • Experience in a medical device/pharmaceutical company or clinical/hospital environment (preferred).
  • Certification by an industry-recognized professional society (e.g., SoCRA, ACRP) or accredited institution (preferred).
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