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The Field Clinical Engineer bridges clinical care and engineering by supporting device use and optimizing functional outcomes for participants in BCI clinical trials. They are responsible for real-time troubleshooting, high-quality data collection, and collaborating with surgeons and internal teams to refine product development.
Requirements
Requires clinical training in PM&R, OT, or PT with 3+ years of experience working with neurological populations and medical devices. Candidates must be familiar with Good Clinical Practice (GCP) and be willing to travel frequently to clinical sites.
Full job description
About Neuralink:
We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world.
Team Description:
The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what’s possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink’s BCI technology for use in people!
Job Description and Responsibilities:
As a Field Clinical Engineer, you will be on the front lines of Neuralink’s clinical programs, working directly with participants, clinicians, and internal teams to translate cutting-edge neurotechnology into meaningful functional outcomes. This role is ideal for individuals with a background in PM&R, occupational therapy, or physical therapy who also have experience in medical devices and thrive in dynamic clinical environments.
You will play a critical role in bridging clinical care, engineering, and research by supporting device use, optimizing participant performance, and ensuring high-quality data collection in both clinical and home settings.
This role requires someone who is hands-on, clinically grounded, technically curious, and able to adapt quickly. You should be comfortable working with participants with significant neurological impairments and motivated by improving independence and quality of life.
In this role, you will:
Work directly with study participants to support device use, training, and optimization during clinical sessions and at home
Apply principles of rehabilitation (PM&R, OT, PT) to maximize participant outcomes and functional performance with the system
Collaborate closely with surgeons, investigators, and site staff to ensure seamless clinical execution across all phases of the study
Serve as the primary interface between participants and the technology, troubleshooting issues in real time and escalating when needed
Support surgical and post-operative workflows, including intraoperative and early post-implant sessions where applicable
Ensure high-quality, protocol-compliant data collection by aligning participant activities with study endpoints and data capture requirements
Partner with clinical, engineering, and data teams to translate real-world use into actionable insights for product and algorithm development
Identify trends in participant performance, usability challenges, and safety signals, and communicate clearly to cross-functional teams
Contribute to development and refinement of training protocols, user workflows, and clinical best practices
Support site onboarding, training, and ongoing engagement to ensure consistency and scalability across clinical sites
Assist in preparation for regulatory inspections and ensure activities are conducted in compliance with GCP, protocol requirements, and internal procedures
Travel to clinical sites as needed to support study execution and participant care
The ideal candidate:
Has a clinical background in PM&R, occupational therapy, or physical therapy, with hands-on experience working with neurological populations (e.g., SCI, ALS, stroke)
Has experience working with medical devices in a clinical or field-based role
Is highly adaptable, proactive, and comfortable operating in a fast-paced, evolving environment
Is technically curious and able to engage with engineers to troubleshoot and improve system performance
Communicates clearly and builds trust with participants, clinicians, and cross-functional teams
Is detail-oriented and understands the importance of protocol adherence and data integrity in clinical research
Required Qualifications:
Clinical training and hands-on experience in PM&R, occupational therapy, or physical therapy, with a focus on neurological populations (e.g., SCI, ALS, stroke)
3+ years of experience in a clinical, field-based, or medical device–adjacent role (rehab, neuromodulation, assistive technology, or similar)
Demonstrated experience working directly with patients and clinicians in dynamic care environments
Strong problem-solving skills with the ability to troubleshoot clinical and technical issues in real time
Ability to interpret participant performance, functional outcomes, and device behavior to inform next steps
Comfort working with technology, including basic data review and interaction with software-driven systems (no need to be a coder, but not afraid of one either)
Working knowledge of clinical research principles, including protocol adherence, endpoint-driven activities, and data quality expectations
Familiarity with Good Clinical Practice (GCP) and general clinical study conduct
Ability to collaborate effectively across clinical, engineering, and operations teams
Strong communication skills, with the ability to engage both participants and highly technical teams
High attention to detail, with the ability to manage multiple participants, sites, and priorities simultaneously
Willingness to travel frequently to support clinical sites and participants
Preferred Qualifications:
Degree or formal training in bioengineering, biomedical engineering, or a related field, with exposure to neurotechnology or implantable systems
Experience working with neuromodulation, brain-computer interfaces, or other neurorehabilitation technologies
Prior experience in a clinical field engineer, clinical specialist, or applications role within a medical device company
Experience supporting surgical procedures, intraoperative environments, or early post-implant programming and troubleshooting
Familiarity with signal-based systems (e.g., neural data, EMG, EEG) and comfort interpreting system performance in real time
Exposure to rehabilitation technology integration, including assistive devices, digital interfaces, or adaptive control systems
Experience supporting multi-site clinical studies or working directly with investigators and study coordinators
Comfort working with data systems (e.g., EDC platforms, basic data visualization tools) to review participant performance and study metrics
Understanding of usability, human factors, and patient-centered design principles
Prior involvement in training clinicians or participants on device use and workflows
Experience working in early-stage or rapidly evolving clinical programs where processes are still being defined
Expected Compensation:
The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees.
Base Salary Range:
$89,000—$250,000 USD
What We Offer:
Full-time employees are eligible for the following benefits listed below.
An opportunity to change the world and work with some of the smartest and most talented experts from different fields
Growth potential; we rapidly advance team members who have an outsized impact
Excellent medical, dental, and vision insurance through a PPO plan
Neuralink is developing ultra-high bandwidth brain-machine interfaces to connect humans and computers.
Industry
Biotechnology Research
Company size
201-500 employees
Founded
2016
Headquarters
Austin, TX
LinkedIn followers
418,601
Total funding
$1.3B
Neuralink is a neurotechnology company building a generalized input/output platform for the brain. Our work has the potential to restore autonomy to those with unmet medical needs and fundamentally transform how humans interact with the world.
Our core technology is an implantable brain-computer interface with ultra-thin, flexible electrode threads placed precisely by a surgical robot, enabling high-bandwidth, bidirectional interaction with neural signals.
We’ve received multiple FDA Breakthrough Device designations and are conducting clinical trials around the world. Trial participants are exploring how our implant could enhance their daily lives — controlling digital devices like computers and smartphones, operating physical devices like robotic arms and wheelchairs, and translating thought directly into speech and text.
Developing brain-computer interfaces is an interdisciplinary challenge, and we’re looking for exceptional talent across engineering, science, and operations. Explore opportunities to contribute to our mission at neuralink.com/careers.
Offices: Austin, TX, US · South San Francisco, California, US