neuralink

Clinical Research Associate

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At a Glance

Location
Austin, Texas, United States
Experience
5+ years
Department
Clinical
Posted
2026-07-29T14:05:33-04:00

Key Requirements

Required Skills

GCP

Domain Knowledge

  • Clinical
  • Education
  • Engineering
  • Insurance
  • Medical

Benefits & Perks

Health Insurance

edical, dental, and vision insurance through a PPO plan Paid holidays Commut

Requirements

5+ years of clinical research experience (device experience strongly preferred)

Working knowledge of GCP (ICH E6), ISO 14155, and applicable FDA regulations

Experience with electronic data capture (EDC) systems and clinical trial documentation

Strong understanding of clinical trial processes, including monitoring and site management

Experience in neuromodulation, implantable devices, or other Class III medical devices

Experience supporting IDE or PMA clinical studies

Responsibilities

As a Clinical Research Associate, you'll play a crucial role in pioneering groundbreaking clinical studies.

Your work will directly contribute to the planning, execution, and success of innovative trials, from the initial phases of study setup to hands-on clinical monitoring and site management.

Collaborating closely with a passionate, cross-functional team, as well as external partners, you'll be at the forefront of Neuralink's mission to push the boundaries of what’s possible in clinical research.

Conduct site initiation, interim monitoring, and close-out visits (remote and on-site)

Ensure clinical studies are conducted in accordance with protocol, GCP, ISO 14155, and applicable regulatory requirements (e.g., 21 CFR Part 812)

Verify the accuracy, completeness, and consistency of clinical trial data through source data verification (SDV) and source data review (SDR)

Team

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!