Preclinical Study Coordinator at Neuralink

<div class="content-intro"><p><strong>About Neuralink:</strong></p> <p>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.</p></div><p><strong>Team Description:</strong></p> <p>The Preclinical Team is responsible for designing, conducting, documenting, analyzing, and reporting preclinical studies. Our team provides a means for ensuring the safe, effective, and robust implantation of Neuralink devices into animals and, ultimately, humans.</p> <p><strong>Job Description and Responsibilities:</strong></p> <p>The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of day-to-day coordination, scheduling, data compilation, and administrative tasks, enabling the Study Director to focus on scientific oversight, data interpretation, and regulatory compliance. The Study Coordinator acts as a key liaison across the preclinical team, technical staff, and cross-functional groups to ensure studies progress smoothly, on time, and in compliance with protocols and SOPs. The Study Coordinator will:<strong><br></strong></p> <ul> <li>Support the Study Director in developing study protocols, amendments, and related documentation.</li> <li>Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings.</li> <li>Identify and help eliminate roadblocks that could delay study progress.</li> <li>Assist with implementation of test methods and practices described in the study protocol and SOPs.</li> <li>Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified.</li> <li>Manage the study schedule, alerting the Study Director and team to critical data collection points or deadlines.</li> <li>Support the documentation and addressing of self-reported or QAU-generated deviations that may affect study quality.</li> <li>Compile data, organize contributing scientist reports, and assist in preparing the final study report so it accurately reflects study results.</li> <li>Maintain organized study files, track communications, and support archiving of data, documentation, protocols, specimens, and reports per GLP.</li> <li>Coordinate day-to-day study activities with technical staff, veterinary teams, and external partners (e.g., CROs if applicable).</li> <li>Contribute to internal tracking systems, meeting minutes, and status updates for the Preclinical Team.</li> </ul> <p><strong>Required Qualifications: </strong><strong><br></strong></p> <ul> <li>Bachelor’s degree&nbsp; in biology, neuroscience, biomedical engineering, animal science, or a related field.</li> <li>Minimum 1 year of experience in preclinical research support, study coordination, or project management (academic experience applies).</li> <li>Solid understanding of GLP regulations (21 CFR Part 58), basic knowledge of ISO 10993, and familiarity with in vivo animal studies.</li> <li>Strong organizational and project management skills with proven ability to manage timelines and multiple priorities.</li> <li>Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft Office (or equivalent) tools.</li> <li>Experience working in or supporting animal research facilities with IACUC protocols.</li> </ul> <p><strong>Preferred Qualifications:</strong><strong> </strong><strong><br></strong></p> <ul> <li>Master’s degree&nbsp; in biology, neuroscience, biomedical engineering, animal science, or a related field.</li> <li>Direct experience with neural device implantation studies or neurosurgical models.</li> <li>Background in a CRO or medical device preclinical setting.</li> <li>Familiarity with electronic data capture systems or GLP-compliant documentation platforms.</li> </ul> <p><strong>Additional Requirements and Competencies:</strong></p> <ul> <li>Willingness to work in an animal research facility environment (with required training and PPE).</li> <li>Flexibility in schedule to support critical study timepoints.</li> </ul><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p><strong>Expected Compensation:</strong></p> <p>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.</p></div><div class="title">Base Salary Range:</div><div class="pay-range"><span>$31</span><span class="divider">&mdash;</span><span>$53 USD</span></div></div></div><div class="content-conclusion"><div> <p><strong>What We Offer:</strong></p> <p>Full-time employees are eligible for the following benefits listed below.</p> <ul> <li>An opportunity to change the world and work with some of the smartest and most talented experts from different fields</li> <li>Growth potential; we rapidly advance team members who have an outsized impact</li> <li>Excellent medical, dental, and vision insurance through a PPO plan</li> <li>Paid holidays</li> <li>Commuter benefits</li> <li>Meals provided</li> <li>Equity (RSUs) <em>*Temporary Employees &amp; Interns excluded</em></li> <li>401(k) plan <em>*Interns initially excluded until they work 1,000 hours</em></li> <li>Parental leave <em>*Temporary Employees &amp; Interns excluded</em></li> <li>Flexible time off <em>*Temporary Employees &amp; Interns excluded</em></li> </ul> </div></div>