Fraustina Hsu
About Fraustina Hsu
Fraustina Hsu is the Assistant Director of QA & Education at the Perlmutter Cancer Center Clinical Trials Office, NYU Langone Health, with extensive experience in clinical research and regulatory compliance.
Current Title and Role
Fraustina Hsu serves as the Assistant Director, QA & Education, at Perlmutter Cancer Center Clinical Trials Office, NYU Langone Health. Since 2019, she has been contributing to the quality assurance and educational aspects of clinical trials, ensuring that all research activities adhere to established standards and guidelines.
Work Experience at NYU Langone Health
Fraustina Hsu began her tenure at NYU Langone Health in 2016 as a Quality Assurance Specialist, a role she held for six months. She then advanced to Quality Assurance Manager, a position she held for three years until 2019. Currently, she serves as the Assistant Director, QA & Education, at the Perlmutter Cancer Center Clinical Trials Office. Throughout her time at NYU Langone Health, she has been instrumental in maintaining compliance and improving the quality of clinical trials.
Previous Positions and Experience
Before joining NYU Langone Health, Fraustina Hsu garnered extensive experience in various roles. She worked as a Data Control Coordinator at Weill Cornell Medical College for 11 years, from 2005 to 2016. Earlier in her career, she was a Clinical Project Assistant at ICON Clinical Research, from 2002 to 2004, and an Administrative Assistant at Cornell University, from 1998 to 2002. Each of these roles contributed to her comprehensive understanding of clinical research and compliance.
Educational Background
Fraustina Hsu earned her Bachelor of Science degree in Applied Economics and Management from Cornell University, College of Agricultural and Life Sciences. Her academic background provided a solid foundation for her career in clinical research and quality assurance, equipping her with essential skills in data management and organizational leadership.
Expertise in Clinical Research and Quality Assurance
Fraustina Hsu possesses extensive experience in both pharmaceutical and hospital settings, allowing her to develop a deep understanding of clinical research. She is well-versed in IRB regulations and federal guidelines, ensuring compliance in human subject research. Additionally, she excels in creating and managing research databases, and her strong organizational and interpersonal skills enable her to lead and collaborate effectively within research teams. Her specialization in regulatory compliance and quality assurance ensures that clinical trials meet all necessary standards and guidelines.