Clinical Research Coordinator

About NudgeAt 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 RoleManage the participant recruitment process end-to-end, from first contact through prescreening, screening, and consentMaintain and report up-to-date recruitment metricsServe as the main point of contact for participants in clinical trialsAssist with adverse event documentation and reportingAssist in writing and updating clinical study documents (CRFs, SOPs, study protocols, ICFs)Support IRB and other regulatory submissionsDevelop trial recruitment and other participant-facing materials in accordance with Good Clinical Practice (GCP) guidelinesAbout YouWe 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 similarExperience in a patient-facing role in clinical trialsExperience writing clear and high quality documentationKnowledge of basic medical terminologyStrong organizational and communication skillsDemonstrated history of exceptional contribution