Preclinical Study Coordinator

Responsibilities

• Support the Study Director in developing study protocols, amendments, and related documentation
• Facilitate cross-functional communication and track study timelines
• Identify and eliminate roadblocks to study progress
• Assist with implementation of test methods and practices described in protocols and SOPs
• Ensure experimental data and observations are accurately recorded and verified
• Manage study schedules and critical data collection deadlines
• Support documentation and addressing of study deviations
• Compile data and assist in preparing final study reports
• Maintain organized study files and support archiving per GLP
• Coordinate day-to-day activities with technical staff, veterinary teams, and external partners

Requirements

• 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)
• Basic knowledge of ISO 10993 and familiarity with in vivo animal studies
• Strong organizational and project management skills
• Proficiency in data compilation and Microsoft Office
• Experience working in or supporting animal research facilities with IACUC protocols

Preferred Qualifications

• Master’s degree in a related scientific field
• Direct experience with neural device implantation studies or neurosurgical models
• Background in a CRO or medical device preclinical setting
• Familiarity with electronic data capture systems or GLP-compliant documentation platforms

About the Company

Neuralink is creating devices that enable a bi-directional interface with the brain to restore movement to the paralyzed, restore sight to the blind, and revolutionize human-digital interaction.