Director of Clinical Operations

Senseye$180K — $205K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant field; Master's or PhD preferred
  • 5-8+ years of experience in clinical research or operations
  • Proven track record of leading clinical teams or managing vendors
  • Experience in medtech, digital health, or neurotechnology
  • Familiarity with FDA clinical/regulatory pathways
  • Strong collaboration and communication skills

Responsibilities

  • Lead and execute clinical studies from initial validation to pivotal trials
  • Oversee and mentor clinical operations team members
  • Manage coordination with external partners like CROs and investigators
  • Design study protocols and generate evidence for regulatory goals
  • Collaborate with Research, AI, and Regulatory teams
  • Support FDA submissions and clinical documentation
  • Contribute to scientific publications and presentations

Benefits

  • Freedom and trust to define your role
  • Flexible paid time off including vacation and sick leave
  • Flexible schedules
  • Comprehensive company health care plan including dental and vision
  • 401k plan
  • Commuter benefits for transportation
  • Mothers' room
  • Fully stocked kitchen offerings
  • Opportunities for continuing education
Full Job Description
Role Description

We are seeking a Director of Clinical Operations to lead the execution of clinical programs supporting product validation, regulatory submissions, and commercialization. This role combines strategic oversight with hands-on execution and includes direct management of clinical operations personnel and external partners. You will play a key role in building and scaling our clinical capabilities as the company grows.

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

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 Have

  • 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

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


The compensation for this role is $180,00 - $205000 annually.

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