Neuralink is developing ultra-high bandwidth brain-computer interfaces to connect humans and computers. We are building a team of multidisciplinary experts passionate about making a world-changing impact.

Neuralink is seeking an exceptional Study Manager to join our Preclinical & Translational Research team. In this role, you will interact with Neuralink’s technical and clinical teams, as well as senior staff, to ensure that preclinical R&D and safety studies are carried out, critical data is gathered to support regulatory filings, and methods comply with good laboratory practices (GLP). You will work closely with a Study Director to compile data, handle reporting, communicate cross-functionally, establish timelines, and eliminate road-blocks that halt progress. This role involves frequent collaboration with the Histology, Animal Care, Product, Quality Assurance, and Study & Surgical Operations teams.

You must thrive in an intense, mission-driven, and collaborative environment.

About You:

• You are a serious thinker who uses a First Principles approach to identifying issues and solving problems quickly.
• You are organized and can work independently.
• You find large challenges exciting and enjoy discovering and defining problems as much as solving them.
• You deliver results consistently. You may enjoy thoughtful conversations about problems and perfecting designs, but in the end, you know that what matters is delivering high quality research reports.
• You are a cross-disciplinary team member. You are excited to work with and learn from software, mechanical, electrical, materials, bioengineers, and neuroscientists. You are comfortable communicating across teams.
• Resourceful, flexible and adaptable; no task is too big or too small.

Key Qualifications:

• Evidence of exceptional ability in neuroscience, biomedical engineering or a related field.
• 4 years of academic or industry experience.
• Experience working in neurobiology, including experimental and analytical design.
• A strong understanding of the scientific method and engineering first principles.
• Demonstrated ability to manage a project, lab, or study.
• Exceptional technical writing abilities.
• Data analysis.

Preferred Qualifications:

• Experience with GLP and FDA guidelines for implantable medical devices.
• Experience working alongside engineers, scientists, veterinarians, and medical doctors.