Manage day-to-day planning and execution of clinical studies for robotic/AI-based products
Partner with clinical sites, CROs/vendors, and internal teams to deliver on time and within budget
Site startup, training, equipment logistics, data management, and issue resolution
Travel within US and occasional international travel; prefer San Carlos, CA onsite with travel as

🎯 Requirements

3+ years clinical trial operations in medical devices/diagnostics
Experience coordinating multi-site studies with CROs/vendors
GCP/ICH knowledge and TMF/documentation experience
Strong project management and stakeholder management skills
Bachelor’s degree in life sciences or related field; advanced degree a plus

🎁 Benefits

Competitive compensation; base pay and incentives
Equal opportunity employer
Onsite/hybrid work options with possible travel

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