Creating a generalized brain interface to restore autonomy to those with unmet medical needs today and unlock human potential tomorrow. Backed by Lightspeed, Sequoia and Founders Fund.
About the role
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.
What they're looking for
- Bachelor’s degree in biology, neuroscience, biomedical engineering, animal science, or a related field
- Minimum 1 year of experience in preclinical research support, study coordination, or project management (academic experience applies)
- Solid understanding of GLP regulations (21 CFR Part 58), basic knowledge of ISO 10993, and familiarity with in vivo animal studies
- Strong organizational and project management skills with proven ability to manage timelines and multiple priorities
- Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft Office (or equivalent) tools
- Experience working in or supporting animal research facilities with IACUC protocols
More about this role
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.
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.
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...
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