Clinical Research Associate

requirements (e.g., 21 CFR Part 812) Verify the accuracy, completeness, and consistency of clinical trial data through source data verification (SDV) and source data review (SDR) Monitor participant safety by reviewing adverse events (AEs), serious adverse events (SAEs), and device deficiencies for completeness and timeliness Ensure sites maintain adequate regulatory documentation, including Investigator Site Files (ISF), informed consent forms, and essential documents Track site performance, enrollment, and data quality metrics; proactively identify risks and implement mitigation strategies Support site training on protocol, investigational device use, and study procedures Collaborate cross-functionally with Clinical Operations, Data Management, Regulatory, and Quality teams Ensure timely resolution of data queries and protocol deviations Prepare and maintain monitoring reports and follow-up letters in accordance with timelines Support audit and inspection readiness at the site level Required

Qualifications: Bachelor’s degree in life sciences, engineering, or related field 5+ years of clinical research experience (device experience strongly preferred) Working knowledge of GCP (ICH E6), ISO 14155, and applicable FDA regulations Experience with electronic data capture (EDC) systems and clinical trial documentation Strong understanding of clinical trial processes, including monitoring and site management Excellent communication, organization, and problem-solving skills Ability to work independently in a fast-paced, evolving environment Up to 30% travel (domestic and occasional international) Preferred

Qualifications: Experience in neuromodulation, implantable devices, or other Class III medical devices Experience supporting IDE or PMA clinical studies Familiarity with risk-based monitoring approaches Exposure to early feasibility or first-in-human studies Exposure to market approval studies Willingness and ability to travel up to 30–50% (domestic and occasional international) Expected

Compensation: The anticipated base salary for this position is expected to be within the following range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. We also believe in aligning our employees’ success with the company's long-term growth. As such, in addition to base salary, Neuralink offers equity

compensation (in the form of Restricted Stock Units (RSU)) for all full-time employees. Base Salary Range: $89,000 — $148,000 USD What We Offer: Full-time employees are eligible for the following

benefits listed below. An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter

benefits Meals provided Equity (RSUs) *Temporary Employees & Interns excluded 401(k) plan *Interns initially excluded until they work 1,000 hours Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded

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