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Paradromics · 1 day ago

Clinical Research Assistant

Austin, TX

Full-time

Onsite

Entry, Mid Level

1+ years exp

Paradromics is building a brain-computer interface (BCI) platform to record brain activity and translate thought into treatments. The Clinical Research Assistant will support the execution of clinical studies, ensuring operations are organized and compliant while managing documentation and data.

BiotechnologyMedicalMedical DeviceNeuroscience

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

Qualification

Clinical research experienceClinical Practice (GCP)Clinical documentation managementRegulatory documentation familiarityAttention to detail

Required

Bachelor's degree in life sciences, health sciences, nursing, biomedical engineering, or a related field (or equivalent clinical research experience)

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