Job Description

About Nudge
At Nudge, our mission is to develop the best technology for interfacing with the brain to improve people's lives. We're starting with an approach that we believe can help the most people the fastest, and also allow us to learn as much about the brain as possible: developing a non-invasive, ultrasound-based device that can stimulate and image the brain at high resolution and depth. This is a vertically integrated effort building cutting-edge hardware, software, and research capabilities to create products that can benefit millions — and eventually billions — of people.
We’ve brought together a team of the best, who believe hard things are worth doing. To succeed, we need to assemble world-class teams across everything we do. We hire people who are exceptional at their craft, do the real work, and execute relentlessly — people who expect the highest levels of both rigor and integrity from each other.
About The Role
Manage the participant recruitment process end-to-end, from first contact through prescreening, screening, and consent
Maintain and report up-to-date recruitment metrics
Serve as the main point of contact for participants in clinical trials
Assist with adverse event documentation and reporting
Assist in writing and updating clinical study documents (CRFs, SOPs, study protocols, ICFs)
Support IRB and other regulatory submissions
Develop trial recruitment and other participant-facing materials in accordance with Good Clinical Practice (GCP) guidelines
About You
We have preference for at least 2 years of professional experience. Regardless of your career level, you should have:
Bachelor’s degree in a STEM field or similar
Experience in a patient-facing role in clinical trials
Experience writing clear and high quality documentation
Knowledge of basic medical terminology
Strong organizational and communication skills
Demonstrated history of exceptional contribution

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