Job Description
📋 Description Manage end-to-end trial execution for assigned studies. Own study plans: timelines, milestones, enrollment projections. Coordinate CROs and vendors; manage scope and budgets. Drive milestones ensuring timely site activation and data quality. Coordinate equipment deployment and site logistics. Ensure trial compliance with GCP/ICH and quality standards. 🎯 Requirements 3+ years of hands-on clinical trial ops in medical devices or diagnostics. Experience coordinating multi-site studies with CROs/vendors. Knowledge of GCP/ICH, essential trial docs, and TMF readiness. Strong project management; ability to drive fast-paced execution. Bachelor's degree in life sciences or related field; advanced degree a plus. 🎁 Benefits Vaccination requirements may apply depending on role. Intuitive is an Equal Opportunity Employer. Export controls may apply to some roles; details provided if applicable.
