About the Role
Role details below.
Responsibilities
- Manage day-to-day execution of clinical validation studies, investigator-led research, and data collection initiatives
- Coordinate with clinical sites on study protocols, patient enrollment, data submission timelines, and compliance requirements
- Maintain study trackers, timelines, and milestone dashboards; surface risks and dependencies proactively
- Oversee site onboarding, training, and ongoing communication for multi-site studies
- Manage clinical data collection workflows, ensuring data integrity, completeness, and traceability
- Coordinate data transfer, de-identification, and integration with engineering and ML teams for model training and validation
- Support development and maintenance of clinical data agreements, IRB submissions, and ethical approvals
- Track and resolve data quality issues across sites and studies
- Prepare and maintain clinical study documentation: protocols, informed consent forms, study reports, and site files
- Support regulatory submissions with clinical evidence summaries, study narratives, and data packages
- Ensure all clinical programs comply with applicable regulatory requirements, GCP guidelines, and internal QMS processes
- Serve as the primary operational liaison between the medical team, product, engineering, and quality functions
- Coordinate medical team inputs into product development, feature validation, and clinical feedback loops
- Support preparation of scientific communications, abstracts, and presentations with clinical data and study results
- Manage vendor relationships for clinical services (CROs, imaging core labs, data management platforms)
Compensation
Competitive equity package with equity upside
Work Arrangement
Remote (Worldwide)
