Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world’s first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Be part of our mission to transform healthcare, improve lives, and drive meaningful change with Noctrix Health.
Noctrix Health is redefining the treatment of chronic neurological disorders with clinically validated therapeutic wearables. Our team of medical device specialists, neuroscientists, and consumer electronics engineers is dedicated to delivering prescription-grade therapy with an outstanding user experience. We have pioneered the world’s first drug-free wearable therapy, clinically proven to alleviate symptoms in adults with drug-resistant Restless Legs Syndrome (RLS). Be part of our mission to transform healthcare, improve lives, and drive meaningful change with Noctrix Health.
We are seeking an experienced and hands-on Senior Clinical Research Scientist to lead the strategy and execution of clinical research supporting the development and validation of emerging therapeutic technologies. This role will have direct responsibility for designing and leading human-subjects research studies, developing study protocols and analysis plans, supporting participant-facing study execution, managing external research collaborations, analyzing clinical and physiological data, and communicating scientific findings through grants, publications, and conference presentations.
The ideal candidate is a highly collaborative scientist who is equally comfortable developing research strategy and working directly with study participants, investigators, research sites, Clinical Affairs, Engineering, and other cross-functional partners. This individual will play a critical role in translating clinical research findings into meaningful product insights, clinical evidence, and future research opportunities.
This is a full-time, hybrid position based in Pleasanton, CA, with a minimum of three days onsite per week, or more depending on business needs. Candidates currently outside the Bay Area who are willing to relocate are encouraged to apply. Travel is expected to be approximately 10%.
Responsibilities
Design and lead multiple prospective human-subjects clinical research studies in parallel, from study concept and protocol development through execution, analysis, and reporting
Develop research strategies, study plans, protocols, case report forms, statistical analysis plans, and other scientific documentation that produce meaningful and operationally feasible data
Provide hands-on support for participant-facing research activities, including study procedures, physiological data collection, protocol adherence, participant safety, and issue resolution
Prepare and support IRB, IDE, ethics committee, and other research-related regulatory submissions as applicable
Lead the analysis and interpretation of clinical and physiological data sets
Collaborate with Engineering and data-science partners to develop analytical methods and, when appropriate, proof-of-concept algorithms that generate clinically meaningful insights
Partner with Engineering and research teams to ensure the reliable collection, quality, and interpretation of physiological and clinical data
Partner closely with Clinical Affairs, Engineering, Product, Regulatory, and other cross-functional teams to support research and product-development priorities
Develop and manage partnerships and collaborations with investigators, research sites, subject matter experts, and other external research partners
Provide training, technical guidance, and ongoing support to investigators, research sites, and external research partners
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