GLP Preclinical Study Coordinator - Growth & Equity

Neuralink; Austin (TX); On-site; USD 66,000 - 110,000; Full time

Benefits offered by this job

Excellent medical, dental, and vision

Paid holidays

Equity (RSUs)

Job summary

Neuralink is seeking a Study Coordinator to provide operational and project management support for GLP-regulated preclinical studies. You will liaise across preclinical teams, technical staff, and external partners to keep studies on schedule, compliant, and well-documented.

The role requires a Bachelor’s degree in a related field and at least 1 year of preclinical coordination or project management experience, with strong organizational and data management skills.

Qualifications

• Bachelor’s degree in biology, neuroscience, biomedical engineering, animal science, or related field.
• Minimum 1 year of experience in preclinical research support, study coordination, or project management.
• Solid understanding of GLP regulations (21 CFR Part 58) and ISO 10993 familiarity.
• Strong organizational and project management skills with ability to manage timelines.
• Experience with animal research facilities and IACUC protocols.

Responsibilities

• Coordinate day-to-day study activities with staff, veterinary teams, and CROs if applicable.
• Support Study Director in developing study protocols, amendments, and documentation.
• Facilitate cross-functional communication and track study timelines and milestones.
• Record observations and data accurately and ensure compliance with protocols and SOPs.
• Prepare final study reports reflecting results and ensure proper archiving.

Skills

Project management

GLP regulations

Data compilation

Organizational skills

Communication

Education

Bachelor’s degree in biology / related field

Master’s degree (preferred)

Tools

Microsoft Office

Electronic data capture systems

Job description

Neuralink is seeking a Study Coordinator to provide operational and project management support for GLP-regulated preclinical studies. You will liaise across preclinical teams, technical staff, and external partners to keep studies on schedule, compliant, and well-documented.

The role requires a Bachelor’s degree in a related field and at least 1 year of preclinical coordination or project management experience, with strong organizational and data management skills.