P

Paradromics

Develops implantable brain-computer interfaces

Field Clinical Specialist/Engineer

Full-Time
No salary listed
Mid
Bachelor's
Austin, TX, USA
In PersonRequires extensive travel to U.S. clinical sites, including study activities outside standard business hours.
Biology & BiotechClinical Research Operations

About the job

Requirements
  • A bachelor's degree in engineering, neuroscience, nursing, biomedical sciences, or another relevant technical or clinical discipline, or an equivalent combination of education and hands-on experience.
  • Hands-on experience working with complex technology in clinical, research, or other human-facing environments, with the ability to learn and operate technical systems independently.
  • Strong technical aptitude and curiosity, including the ability to understand system behavior, investigate problems, and troubleshoot across hardware, software, connectivity, and data.
  • Experience working directly with patients, research participants, clinicians, or other end users, with the interpersonal judgment and empathy needed to build trust during repeated interactions.
  • Ability to recognize and assess data or signal-quality issues and work with technical teams to investigate their source.
  • Ability to remain calm, thoughtful, and effective when troubleshooting problems in participant-facing or other high-stakes environments.
  • Strong communication skills, including the ability to translate technical concepts for clinical audiences and clinical or participant experiences for technical teams.
  • Strong attention to detail and ability to consistently follow defined procedures, document observations, and escalate issues appropriately.
  • Willingness and ability to travel extensively to U.S. clinical sites and support study activities that may occur outside standard business hours.
Responsibilities
  • Serve as the in-field technical representative during early feasibility study procedures, study visits, and neural recording sessions, working with participants, clinical site teams, and company colleagues.
  • Prepare, configure, calibrate, operate, and break down study systems, complete system checks, and confirm readiness for clinical and recording sessions.
  • Support the design, execution, and refinement of neural recording and brain-computer interface session workflows to generate high-quality, consistent, and analyzable neural data.
  • Monitor neural signals and system performance in real time and recognize signal loss, artifacts, unexpected behavior, or configuration issues affecting session quality.
  • Troubleshoot hardware, software, device, connectivity, and signal-quality issues in real time within clinical environments, escalating when additional support is needed.
  • Develop an understanding of the relationship between system configuration, neural signals, participant behavior, and task performance to inform experimental workflows and decoding approaches.
  • Identify unexpected system behavior, workflow challenges, usability issues, and emerging risks, and communicate them before they affect participant experience, safety, or study integrity.
  • Capture and communicate field observations, technical issues, failure modes, usability feedback, and system limitations to support engineering improvements and risk-management activities.
  • Build relationships with study participants and their support networks to create a professional, comfortable, and reliable experience during repeated study sessions.
  • Build trust and credibility with investigators, fellows, coordinators, and research staff through preparation, technical competence, sound judgment, responsiveness, and professionalism.
  • Translate real-world clinical and participant experiences into actionable information for Engineering, Clinical Affairs, Data Science, and Quality.
  • Contribute to training materials, field playbooks, standard operating procedures, troubleshooting guides, and workflows for additional sites, field team members, and future studies.
Desired Qualifications
  • Advanced technical, clinical, or scientific training.
  • Experience with neurotechnology or neuroscience systems, including neural signals, brain-computer interfaces, electroencephalography, electrocorticography, microelectrode arrays, neuromodulation, electrophysiology, or neural data-acquisition platforms.
  • Clinical training or experience in nursing, clinical research, rehabilitation, neuroscience, or another patient-facing healthcare discipline.
  • Technical experience with Python, MATLAB, signal processing, time-series data, data visualization, or similar analytical tools.
  • Experience supporting medical devices, complex research equipment, or integrated hardware and software systems in clinical or research environments.
  • Exposure to early feasibility, first-in-human, or small-participant clinical studies with heightened safety and regulatory oversight.
  • Familiarity with good clinical practice, investigational device exemption studies, and academic medical center or investigator-led research environments.
  • Experience contributing to standard operating procedures, field guides, troubleshooting resources, training materials, or onboarding programs.
  • Ability to operate independently in the field while maintaining strong communication and partnership with a broader cross-functional team.

About the company

Paradromics develops implanted brain-computer interfaces to collect and interpret large-scale neural data for neurological disorders. Its Connexus Direct Data Interface (DDI) is a surgically implanted system that records a high volume of individual neural signals and provides data interfaces for therapeutic and diagnostic use. Unlike many BCIs that focus on smaller-scale signals or consumer devices, Paradromics offers an end-to-end medical-grade platform, including installation, maintenance, and data analysis services for medical institutions and researchers. The goal is to broaden treatment options and improve diagnosis by leveraging rich brain data to guide therapies and research.

Company Size

51-200

Company Stage

Series A

Total Funding

$108M

Headquarters

Austin, Texas

Founded

2015

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Simplify Jobs

Simplify's Take

What believers are saying

  • William J. Marks joined as chief clinical officer on July 7, 2026.
  • APEX opened Connexus access to Stanford and other academic collaborators in March 2026.
  • Paradromics keeps hiring in 2026, signaling manufacturing and clinical scale-up after first implantation.

What critics are saying

  • Paradromics still has one human patient; commercial demand remains unproven through 2027.
  • A device infection, seizure, or decoding failure during Connect-One would freeze adoption.
  • Neuralink and Synchron can outrun Paradromics on capital, trials, and clinician mindshare.

What makes Paradromics unique

  • Connexus records single-neuron signals; Paradromics claims world-leading data-rate, August 2026.
  • University of Michigan implanted Connexus first human patient in June 2026.
  • FDA approved Connect-One and broader personal-device connectivity in August 2026.

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Benefits

  • Flexible Work Hours

Growth & Insights and Company News

6 month growth

1%

1 year growth

0%

2 year growth

0%
MD+DI
Oct 19th, 2026
Imaging collaboration aims to improve brain-computer interfaces.

Imaging collaboration aims to improve brain-computer interfaces. Paradromics, Siemens Healthineers build imaging workflow for brain implants Staff Informa Markets Engineering October 19, 2026 Advanced 3T MRI systems from Siemens Healthineers, such as MAGNETOM Cima.X, have the potential to support the growing clinical use of implantable brain-computer interfaces (BCIs). Paradromics is in collaboration with Siemens Healthineers to develop an advanced multimodal imaging platform designed to support the growing clinical use of implantable brain-computer interfaces (BCIs). The companies will develop an integrated imaging approach spanning the continuum of BCI care, from patient candidacy assessment and neural target identification through surgical planning, intraoperative navigation, post-implant localization, neural validation of functional imaging findings, and outcomes assessment. A new imaging workflow for BCI care The collaboration comes at a time when brain-computer interfaces are advancing from academic proof-of-concept research toward clinical systems capable of restoring functions such as communication and computer control. As these systems become more sophisticated, accurately identifying the areas of the brain responsible for speech, movement, and other functions becomes increasingly important to device performance and patient outcomes. "Building the best hardware is only part of the story. BCI performance begins before an implant ever reaches the brain," said Matt Angle, PhD, founder and CEO of Paradromics. "The ability to understand each patient's individual anatomy and functional organization can help us identify the right neural target and place our technology with greater accuracy. Working with Siemens Healthineers will help us streamline this process prior to surgery, so that patients get the best possible outcome." Multimodal imaging meets clinical precision The planned workflow will integrate multiple imaging modalities, including structural MRI, functional MRI, vascular imaging, and CT. Together, these technologies can help clinical teams assess brain anatomy, identify functionally relevant regions, plan surgical trajectories, avoid critical vascular structures, and determine the final location of implanted BCI components. End-to-end imaging workflows will also be developed in cooperation with Paradromics clinical research investigators, including Daniel B. Rubin, MD, PhD, of the Mass General Brigham Neuroscience Institute's Center for Neurotechnology and Neurorecovery. The participation of leading clinical research centers will help ensure the workflow is informed by real-world BCI research and clinical practice as it is refined for broader adoption. "At Siemens Healthineers, we are focused on pioneering breakthroughs in healthcare by transforming imaging into increasingly precise, actionable information for clinicians," said Dr. Donald Hardie, head of Magnetic Resonance at Siemens Healthineers. "Brain-computer interfaces represent an important new frontier for neuroscience. Working with Paradromics gives us the opportunity to explore how advanced multimodal imaging, automation and clinical decision support can help make these procedures more precise, repeatable and ultimately more accessible across leading medical centers." A distinctive element of the collaboration will be the ability to compare functional imaging predictions with neural activity recorded directly from implanted Paradromics devices. Intracortical recordings can provide high-resolution information about the activity of individual neurons and their usefulness for decoding intended speech or movement. Comparing those signals with preoperative imaging could help researchers determine how accurately imaging identifies functionally important brain regions and continually refine imaging and targeting methods for future patients. "Our approach has always been to build the Connexus BCI platform into the existing healthcare ecosystem, working with leaders across the care pathway and using established technologies and clinical workflows wherever they make sense," said William J. Marks, Jr., MD, MS-HCM, Chief Clinical Officer of Paradromics. "We want to make things easy for hospitals, not require them to buy and train on bespoke capital equipment. Siemens Healthineers is the leader in advanced medical imaging, and most hospitals in the US use their systems. This is an obvious opportunity for collaboration." From speech restoration to broader applications The collaboration is expected to initially focus on speech-motor function, building on Paradromics' clinical work in communication restoration. The companies envision extending the approach to additional BCI applications, including hand motor control and language restoration following stroke. Imaging and targeting techniques developed for speech, motor and language applications may also have relevance to visual, auditory and cognitive mapping, as well as broader neurosurgical planning. Informa Markets Engineering Want more MD+DI in your search results?

Medical Device Network
Aug 27th, 2026
Paradromics gets FDA nod for broader BCI device compatibility.

Paradromics gets FDA nod for broader BCI device compatibility. The FDA approval will enable the BCI platform to support more internet-connected personal devices including laptops, tablets and phones. Neurotech company Paradromics has received approval from the US Food and Drug Administration (FDA) to broaden the range of personal computing devices compatible with its investigational brain-computer interface (BCI) system. The authorisation pertains to the company's ongoing Connect-One Early Feasibility Study, which is evaluating the safety and functionality of the Connexus BCI for restoring communication and enabling computer-device control in individuals with severe motor impairment. The FDA approval will enable the BCI platform to support a wider variety of internet-connected personal devices including laptops, tablets and mobile phones. Paradromics intends to implement these changes through its Convey user interface, which is designed to translate decoded neural signals into communication and digital control across supported platforms. Previously, the BCI system was limited to use with company-provided hardware. The approval marks what Paradromics describes as a step towards allowing users with severe motor impairment to interact with the types of devices they use in everyday life. Once Paradromics completes the agreed deployment and testing process, new compatible personal devices could be added without requiring separate approvals for each device. The company stated that this change does not affect the existing clinical care model in the study but offers greater flexibility to assess how BCI-enabled computer control might fit into individual daily digital environments. Paradromics founder and CEO Matt Angle said: "As Medical Device Network think about building BCI as a technology platform, Medical Device Network need to push for generalised connectivity. "That means being able to connect with the products and technology that are already part of your life. This approval begins clearing the way toward a BCI platform that can move with the user rather than tethering him or her to a fixed computing environment." Paradromics is developing its BCI platform to decode neural activity recorded at the level of single neurons, with initial studies focused on restoring communication for people unable to speak due to paralysis and severe motor impairments. The company's stated long-term strategy aims to enable the translation of neural intent into actions across an expanding range of technologies and applications. In March this year, Paradromics initiated a programme to drive academia's access to its BCI to advance innovation in the device space. Give your business an edge with its leading industry insights.

NeuroTech.com
Aug 27th, 2026
Paradromics wins FDA nod to connect its BCI platform to personal devices.

Paradromics wins FDA nod to connect its BCI platform to personal devices. 2026-08-27 Brain-computer interface company Paradromics has secured a pivotal regulatory green light from the U.S. Food and Drug Administration to extend the compatibility of its BCI platform to personal devices, a move that signals a meaningful shift in how neural interface technology can be deployed and accessed in everyday settings. The clearance, confirmed this week, positions Paradromics as one of the first companies to receive explicit regulatory sanction for this class of device integration. What the FDA approval actually means. The FDA's decision to expand Paradromics' device compatibility framework is notable not simply as a business win but as a regulatory precedent. Until now, BCI systems approved for clinical use have largely operated within closed, proprietary hardware ecosystems - purpose-built devices that rarely communicate with the smartphones, tablets, or laptops that patients already own. By granting Paradromics the authority to interface its BCI with personal devices, the FDA is effectively acknowledging a new category of connected neural technology, one where the boundary between clinical hardware and consumer electronics is deliberately blurred. For regulatory affairs professionals across the industry, this approval will become a closely studied template for future submissions seeking similar connectivity permissions. The technology and its implications. Paradromics has long focused on high-bandwidth neural data acquisition, aiming to build systems capable of reading and transmitting neural signals with sufficient fidelity for practical communication and control applications. Extending that capability to personal devices introduces a new layer of practical utility: users could theoretically interact with their own phones or computers directly through their neural interface rather than through dedicated clinical terminals. This kind of ambient usability has been a long-standing goal in the BCI field, but regulatory hesitance around cybersecurity, data privacy, and device safety has historically kept it out of reach. The FDA clearance suggests that Paradromics has addressed enough of those concerns to satisfy regulators, though the specifics of any conditions or labeling requirements attached to the approval remain important details for the industry to monitor. Market context and the road ahead. This development arrives at a moment when the broader BCI sector is navigating intense scrutiny around long-term viability, safety, and real-world usability. Competitors including Synchron and Precision Neuroscience are pursuing their own connectivity and usability expansions, meaning Paradromics' regulatory win could accelerate a race toward personal-device integration across the field. For payers, hospital systems, and rehabilitation technology buyers, the ability to connect a BCI to existing personal hardware also carries meaningful cost implications, potentially reducing the infrastructure burden associated with deploying neural interface technology at scale. As the FDA's comfort with connected neural devices continues to evolve, Paradromics' clearance may well mark the opening of a new regulatory era in which the personal device becomes a standard component of the BCI ecosystem. Stay wired into neurotech BCI breakthroughs, funding rounds, and device clearances - weekly, free.

NeuroTech.com
Aug 26th, 2026
Paradromics wins FDA approval to embed BCI software in personal devices.

Paradromics wins FDA approval to embed BCI software in personal devices. 2026-08-26 The brain-computer interface sector received a significant regulatory signal today as Paradromics secured FDA approval to embed its BCI software within personal devices. The clearance marks a notable shift in how regulators are beginning to treat neural interface software - not as exclusively clinical hardware confined to hospital settings, but as technology capable of operating within the broader personal device ecosystem. For an industry that has long wrestled with the gap between laboratory capability and real-world deployment, this approval represents a meaningful step forward. Why this matters. Regulatory approvals in the BCI space have historically been tied to implantable hardware or tightly controlled clinical platforms. Paradromics obtaining clearance to embed its software into personal devices challenges that convention and opens a new category of regulatory pathway for the industry. The decision signals that the FDA is becoming more comfortable evaluating neural interface software on its own merits, separate from the physical form factor of a dedicated medical device. For other companies developing software-defined BCI solutions, this creates a precedent that could accelerate their own regulatory strategies and reduce the friction historically associated with bringing neural technologies to everyday users. The technology. Paradromics has been developing high-bandwidth neural interface technology with a focus on data throughput - the ability to read and process large volumes of neural signals reliably. Embedding that capability into personal devices suggests the company's software stack has matured to a point where it can operate outside of purpose-built clinical enclosures, relying instead on the processing power and connectivity of existing consumer hardware. This is architecturally significant. Rather than requiring patients or users to adopt entirely new and often expensive dedicated systems, Paradromics' approach could allow neural interface functionality to be delivered through devices people already own and carry. The implications for accessibility, adoption curves, and cost of care are substantial. Market context. Today's approval arrives against a backdrop of intensifying global competition in the BCI space. China has been accelerating its own standardization efforts, with domestic firms increasingly positioning themselves as challengers to established players like Neuralink. Meanwhile, the patent landscape around BCI and humanoid robot integration is drawing new legal and regulatory scrutiny across multiple jurisdictions. In this environment, a U.S. FDA approval for a software-embedded BCI platform carries strategic weight beyond the immediate commercial opportunity for Paradromics - it reinforces the United States as an active regulatory participant in shaping how neural interface technology is defined and governed globally. As BCI software begins to find footing within personal device frameworks, the industry should expect regulatory bodies worldwide to revisit their own classification criteria, potentially unlocking a new wave of software-first neural interface products. Stay wired into neurotech BCI breakthroughs, funding rounds, and device clearances - weekly, free.

Associated Press
Jul 7th, 2026
Paradromics appoints neurologist William J. Marks as chief clinical officer for BCI platform

Paradromics has appointed William J. Marks, Jr., MD, MS-HCM, as chief clinical officer. Dr Marks is a neurologist with nearly three decades of experience in clinical neuroscience, implantable medical devices, and neuromodulation. The appointment comes as Paradromics advances its FDA-approved Connect-One Early Feasibility Study of the Connexus brain-computer interface. Earlier this month, the company announced the first human implantation of the Connexus BCI at University of Michigan Health. Dr Marks will guide clinical strategy, product development, and regulatory planning. He previously served as professor of neurology at UCSF for nearly two decades and held senior clinical leadership roles at Verily Life Sciences from 2016 to 2023. Paradromics develops brain-computer interface technologies designed to restore communication and control for people with neurological conditions.