Jobs at Senseye

Coordinate and execute IRB-approved clinical trial activities: recruit, screen, consent, run participants through experiments, collect and enter study data, maintain records per GCP/HIPAA, liaise with stakeholders, manage study logistics, and support team project management through study completion.

Manage Senseye's virtual site for a Phase III SaMD trial from setup through closeout. Responsibilities include participant recruitment and visits, protocol compliance, regulatory submissions (IRB, consent, AE reporting), data quality assurance, training and supervising staff, timeline and budget management, cross-functional collaboration, and reporting clinical findings to stakeholders.

Lead clinical studies for SaMD products, oversee clinical operations team, manage external partners, ensure compliance, and support FDA submissions.

Design and run analyses of experimental biometric/neuroscience data. Build and review Python analysis pipelines, validate data quality, verify assumptions, and interpret results. Produce clear analysis reports and documentation, present findings to the team, and collaborate with research and data scientists across study design, execution, and interpretation.

The Vice President, Product defines product requirements for a FDA-regulated software medical device, ensuring clinical usability and alignment with market needs while coordinating cross-functional teams toward product commercialization and deployment.