Clinical Research Assistant
Company: Paradromics, Inc.
Location: Austin
Posted on: February 19, 2026
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Job Description:
Job Description Job Description Clinical Research Assistant
About Paradromics Brain-related illness is one of the last great
frontiers in medicine, not because the brain is unknowable, but
because it has been inaccessible. Paradromics is building a
brain-computer interface (BCI) platform that records brain activity
at the highest possible resolution: the individual neuron. AI
algorithms then decode this massive amount of brain-data, enabling
the seamless translation of thought into treatments. Our first
clinical application, the Connexus® BCI, will help people who are
unable to speak, due to progressive neuromuscular diseases and
neural injury such as ALS, spinal cord injuries and stroke, to
communicate independently through digital devices. However, the
capabilities of our BCI platform go far beyond our first
application. With the brain in direct communication with digital
devices, we can leverage technology to transform how we treat
conditions ranging from sensory and motor deficits to untreatable
mental illness. The Role The Clinical Research Assistant (CRA) will
support the successful execution of early feasibility and
first-in-human clinical studies by ensuring clinical operations are
organized, compliant, and progressing on schedule. Reporting to the
Director of Clinical Affairs, this role works closely with clinical
sites, investigators, IRBs, and internal cross-functional teams to
manage documentation, data, and study coordination activities. This
position is well-suited for someone who thrives in fast-moving,
early-stage environments and is excited to help build the clinical
foundation for a novel implantable neurotechnology.
Responsibilities Support day-to-day execution of early feasibility
and first-in-human clinical studies, ensuring study activities
remain organized, compliant, and on track Maintain inspection-ready
clinical documentation, including site files, study logs, training
records, and sponsor files Coordinate site operations such as
screening, follow-up visits, monitoring activities, and reporting
to prevent administrative or documentation-related delays Manage
IRB submissions and ongoing oversight across multiple sites,
including initial submissions, continuing reviews, amendments,
reportable events, and correspondence Track and support study data
quality by assisting with CRF completion, source document review,
and timely query resolution Ensure consistent application of
protocol requirements and Good Clinical Practice (GCP), identifying
deviations or site questions early and escalating as appropriate
Support development and continuous improvement of clinical
trackers, templates, and workflows to improve operational
consistency across sites Communicate clearly and professionally
with investigators, site coordinators, and internal stakeholders
Required Education Bachelor’s degree in life sciences, health
sciences, nursing, biomedical engineering, or a related field (or
equivalent clinical research experience) Required Qualifications
1–3 years of clinical research experience as a Clinical Research
Assistant, Clinical Research Coordinator, or in a similar role,
preferably in medical device studies Strong understanding of
clinical research fundamentals, including GCP, informed consent,
source documentation, CRFs, and site-based study conduct
Demonstrated experience managing clinical documentation, trackers,
and deadlines with a high level of accuracy and attention to detail
Preferred Qualifications Experience supporting early feasibility or
first-in-human studies, including small-N trials and heightened
regulatory oversight Exposure to medical device or neurotechnology
studies, particularly implantable devices (e.g., DBS, SCS,
implantable BCI) Familiarity with regulatory documentation such as
IDE-related materials, IRB submissions, protocol amendments, and
inspection readiness activities Paradromics is an Equal Opportunity
Employer. All qualified applicants will receive consideration for
employment without regard to race, color, religion, sex, sexual
orientation, gender identity, or national origin. Powered by JazzHR
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Keywords: Paradromics, Inc., Temple , Clinical Research Assistant, Science, Research & Development , Austin, Texas