What are the responsibilities and job description for the Clinical Research Coordinator position at Neuralink?
Company Description :
We are creating the future of brain-computer interfaces : building devices now that have the potential to help people with paralysis regain mobility and independence and invent new technologies that could expand our abilities, our community, and our world.
Team Description :
The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what's possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink's BCI technology for use in people!
Job Description & Responsibilities :
As a Clinical Research Coordinator on the Clinical Team, you will help support the larger team at Neuralink responsible for clinical trial operational and regulatory activities. We are looking for someone who is self-driven-able to initiate work independently and meet deadlines with accuracy and efficiency. Our team operates in a dynamic environment, so the ideal candidate will possess a positive attitude, adaptability, and a willingness to take accountability for new responsibilities. Additionally, you will be expected to :
- Serve as the first line of contact with interested clinical trial participants
- Work to grow and maintain our Patient Registry
- Establish and maintain relationships with community partners and patient advocacy groups
- Independently contribute towards trial recruitment activities
- Develop trial recruitment and other participant-facing materials
- Maintain and implement study documentation (e.g., SOP and CRF edits)
- Coordinate interactions and payments and manage communications with external vendors
- Support Neuralink clinical studies by ensuring adherence of trial plans to study protocols as well as ensuring compliance with regulations and standards for clinical research
- Provide regulatory assistance when needed, including but not limited to submitting ethics board submissions and developing safety reports as well as adverse event reportings
Required Qualifications :
Preferred Qualifications :
Pay Transparency :
The following details are for Texas individuals only.
Texas Pay Transparency
80,000-$134,000 USD
For Full-Time Employees, your compensation package will include two major components : salary and equity. Guidance on salary for this role will be determined according to the level at which you enter the organization, with the ability to gain more over time as you contribute. In addition, Full-Time Employees are eligible for the following benefits listed below.
What We Offer :
Salary : $80,000 - $134,000
