💼 About This Role

You'll support Study Directors in GLP-regulated preclinical studies for Neuralink's brain-computer interface devices. You'll handle day-to-day coordination, scheduling, and data compilation to keep studies on time and compliant. This role offers direct impact on revolutionary neurotechnology and growth potential in a fast-moving startup.

🎯 What You'll Do

• Support Study Director in developing study protocols and amendments.
• Facilitate cross-functional communication and track study timelines.
• Coordinate day-to-day activities with technical and veterinary teams.
• Compile data and assist in preparing final study reports.

📋 Requirements

• Bachelor’s degree in biology, neuroscience, biomedical engineering, or related field.
• 1+ year of preclinical research support or study coordination experience.
• Knowledge of GLP regulations (21 CFR Part 58).
• Experience with IACUC protocols and animal research facilities.

✨ Nice to Have

• Master’s degree in a related field.
• Neural device implantation or neurosurgical model experience.
• CRO or medical device preclinical background.

🎁 Benefits & Perks

• 🏥 Excellent medical, dental, vision insurance (PPO plan).
• 📈 Equity compensation (RSUs) for full-time employees.
• 🍽️ Meals provided at work.
• 🚗 Commuter benefits.
• 🏖️ Flexible time off.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical or Team Interview· 60 min