Professional Overview
Thao Vu is an experienced professional currently serving as an Associate Start-up Manager, leveraging expertise in clinical research, operations management, and regulatory affairs to drive business growth and excellence in the industry. Key areas of expertise include clinical trials, site readiness, and regulatory compliance, with a strong focus on the pharmaceutical and biotechnology sectors.
Experience Summary
Current Role
As an Associate Start-up Manager at SMART Research Co., Ltd, and Site Readiness and Regulatory Senior at Fortrea, Thao Vu is responsible for managing start-up activities for clinical trials, ensuring site readiness, and overseeing regulatory compliance. Key responsibilities include coordinating with cross-functional teams, developing and implementing study start-up plans, and ensuring adherence to regulatory requirements. Achievements in this role have included successful site initiation and study start-up, resulting in improved trial efficiency and compliance.
Career Progression
Thao Vu's career progression reflects a steady growth trajectory, with notable previous roles including Safety Operation - Medical Information at IQVIA Asia Pacific, Clinical Research Associate at AstraZeneca, and Operation Manager at VUBI JSC. Key achievements and contributions in these roles have included ensuring patient safety, managing clinical trials, and leading operational teams to achieve business objectives.
Academic Background
Thao Vu's highest level of education is a graduate degree from Seoul National University and Chonnam National University. Relevant specializations include bioscience and biotechnology, with notable academic achievements during the graduate program.
Areas of Expertise
Thao Vu possesses a range of industry-specific skills, technical competencies, and leadership and management capabilities. Expertise includes clinical trials management, site readiness, regulatory compliance, operational management, and team leadership. Technical competencies encompass knowledge of good clinical practice (GCP), regulatory requirements, and clinical trial management systems.
Professional Impact
Notable projects and initiatives have included managing clinical trials, developing and implementing operational plans, and ensuring regulatory compliance. Industry contributions have been focused on advancing clinical research and improving operational efficiency. Measurable achievements have included successful trial completion, improved site readiness, and enhanced regulatory compliance.
Conclusion
Thao Vu's professional trajectory reflects a commitment to excellence in clinical research, operations management, and regulatory affairs. Currently focused on driving business growth and excellence as an Associate Start-up Manager and Site Readiness and Regulatory Senior, Thao Vu offers a unique value proposition as a seasoned professional with expertise in managing clinical trials, ensuring site readiness, and overseeing regulatory compliance.
