Preclinical Study Coordinator

Benefits

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Weekend work

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Application

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About this role

Preclinical Study Coordinator Austin, Texas, United States About Neuralink: 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. Team Description: 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. Job Description and Responsibilities: 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: - Support the Study Director in developing study protocols, amendments, and related documentation. - Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings. - Identify and help eliminate roadblocks that could delay study progress. - Assist with implementation of test methods and practices described in the study protocol and SOPs. - Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified. - Manage the study schedule, alerting

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