Director of Clinical Operations
About The Position
Senseye is a NeuroTechnology Company in Austin, TX, focused on revolutionizing Mental Health by building the world's first Objective Mental Health Diagnostics. Their platform measures cognitive activity via the eye through mobile phones, with diagnostics for PTSD entering clinical trials, followed by Anxiety and Depression. The platform aims to provide clinicians with a safe, objective, and accurate approach to identifying and monitoring mental health disease. This role, Director of Clinical Operations, involves leading and executing clinical studies from early validation through pivotal trials, overseeing and mentoring clinical operations team members, and managing external partners like CROs, sites, and investigators. Key responsibilities include designing study protocols, generating evidence for regulatory and commercial goals, collaborating with Research, Artificial Intelligence, and Regulatory teams, supporting FDA submissions and clinical documentation, contributing to scientific publications, and ensuring compliance with GCP and applicable regulations.
Requirements
- Bachelor’s degree in a relevant field (Master’s or PhD preferred)
- 5–8+ years of experience in clinical research, clinical operations, or clinical affairs
- Demonstrated experience leading or managing clinical teams or vendors (e.g., CROs)
- Experience in medtech, digital health, or neurotechnology
- Familiarity with FDA clinical/regulatory pathways
- Strong cross-functional collaboration and communication skills
Nice To Haves
- Experience in mental health or neuroscience
- Background in digital biomarkers or AI-driven diagnostics
- Startup or high-growth company experience
- Experience building or scaling clinical operations functions
Responsibilities
- Lead and execute clinical studies from early validation through pivotal trials
- Oversee and mentor clinical operations team members, fostering strong execution and professional development
- Manage and coordinate external partners, including CROs, sites, and investigators
- Design study protocols and generate evidence to support regulatory and commercial goals
- Collaborate cross-functionally with Research, Artificial Intelligence, and Regulatory teams
- Support FDA submissions and clinical documentation
- Contribute to scientific publications and presentations
- Ensure compliance with GCP and applicable regulations
Benefits
- The freedom and trust to define your role as we design, build, and ship our products
- Competitive salary and stock option plan
- Flexible paid time off (vacation, sick leave, and public holidays)
- Flexible schedules
- Company health care plan
- Medical, dental, and vision insurance
- Short and long term disability insurance
- Life insurance policy
- 401k
- Commuter benefits for parking, public transit, carshares, etc.
- Mothers' room
- Fully stocked kitchen
- Opportunities for continuing education
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What This Job Offers
Job Type
Full-time
Career Level
Director
Number of Employees
1-10 employees
