Clinical Research Coordinator

Boston, MA (Monday through Saturday On-Site) Our client is a Boston-based brain-computer interface company currently in stealth mode, working to improve human lives through non-invasive neurotechnology. They develop precision brain-stimulation devices and are conducting clinical research across sleep, reasoning, mood, and related human outcomes. The team is building the clinical infrastructure to test ideas quickly, rigorously, and at scale. They currently have two devices in clinical trials and are looking for highly capable people who want to do difficult, meaningful work alongside an ambitious early-stage team. About the Role As a Clinical Research Coordinator, you will run human studies from day-to-day execution through data collection and operational coordination. You will work directly with study participants, operate non-invasive research devices following approved protocols, collect high-quality data, and help improve the systems that allow the company to launch and execute studies rapidly. This role does not require a traditional clinical-research background. We are open to candidates from healthcare, research, operations, customer-facing, technical, or other high-performance environments. What matters most is your ability to learn quickly, work carefully, take ownership, and follow through. Responsibilities Execute human research studies in accordance with approved protocols, safety procedures, and study requirements. Prepare research spaces, devices, materials, and documentation for participant visits. Guide participants through study visits professionally, clearly, and empathetically. Set up and operate non-invasive stimulation devices after completing training. Collect, enter, organize, and quality-check study data and source documentation. Support participant recruitment, screening, scheduling, consent processes, and follow-up as needed. Monitor studies for operational issues, protocol deviations, participant concerns, or safety events, and escalates them promptly. Coordinate with clinical, scientific, and operations teammates to keep studies moving efficiently. Contribute to experimentation, process improvement, and the development of scalable clinical workflows. Adapt to new protocols, research questions, and operating priorities as the company evolves. Qualifications Strong learning agility and the ability to become effective quickly in unfamiliar situations. High personal accountability, reliability, and follow-through. Meticulous attention to detail, particularly when following structured procedures and documenting work. Excellent judgment and comfort raising concerns when something appears incorrect, unclear, or unsafe. Strong interpersonal skills and the ability to make participants feel comfortable and respected. A practical, no-ego working style: willing to do both routine operational work and solve unstructured problems. Motivation to work in an intense, fast-moving startup environment focused on meaningful human challenges. Comfort working with technology, data-entry systems, and new tools. Preferred Skills Experience in clinical research, human-subject research, healthcare, emergency medicine, nursing, medical assisting, laboratory operations, or research coordination. Experience in a high-throughput operational environment, such as an emergency department, hospital, research site, or high-volume service setting. Familiarity with informed consent, IRB-regulated research, GCP, HIPAA, study documentation, or participant-facing research. Experience interacting directly with patients, research participants, or customers. #J-18808-Ljbffr RecruitSeq