Jade Cao

Director, Clinical Operations @ Third Harmonic Bio

About

As an experienced professional in clinical operations, I bring a wealth of skills and expertise to the table. With a meticulous focus on ensuring compliance with FDA regulations, ICH GCP guidelines, and SOPs/Quality. I have successfully managed all aspects of clinical trials, from protocol development to start up, maintenance and closing. My strong leadership abilities have enabled me to effectively lead study teams and foster cross-functional collaboration with external partners. I excel in project management, providing oversight across all study phases and coordinating multiple interfaces to optimize study planning and execution. With excellent communication and negotiation skills, I adapt my approach to effectively address various stakeholders and encourage collaboration within and beyond the team. Adept at problem-solving and decision-making, I anticipate and mitigate study risks while proactively identifying opportunities for improvement. My commitment to operational excellence and people development ensures that projects are delivered on time, with the highest quality, and within budget.

Country

United States

City

Greater Boston

Industry

Biotechnology

Skill

Clinical Research, Electronic Data Capture (EDC), Analytical Skills, Research and Development (R&D), Clinical Development, Good Clinical Practice (GCP), Project Management, Clinical Trials, Microsoft Office, Microsoft Excel, Microsoft Word, Phlebotomy, Vital Signs, EKG, PowerPoint, Team-oriented, Always Willing to Learn, Diplomatic History, IRB, Research

Experience

Director, Clinical Operations

Third Harmonic Bio

2024-6 - Present · 2 yrs 4 mos

Lead Global Study Manager

Sanofi

2022-10 - 2024-6 · 1 yr 9 mos

Cambridge, Massachusetts, United States

• Lead the planning, management, and execution of clinical studies and programs within Trial Operations. • Drive the achievement of operational objectives, ensuring all trial deliverables are met on time, within budget, and with the highest quality standards. • Prepare study-related plans and materials, identify risks, and develop contingency plans. • Manage study planning, budget, and execution while ensuring compliance with GCP/ICH, SOPs/QDs. • Coordinate cross-functional study teams, including internal and external resources. • Organize internal team meetings and oversee vendors for study execution. • Manage Clinical and Medical Service Providers, ensuring adherence to scope of work, timelines, and budget. • Demonstrate excellent written and oral communication skills, critical-thinking/problem-solving abilities, and strong leadership to drive operational success.