Caro U.
About Caro U.
Caro U. is a Clinical Operations professional at Asher Biotherapeutics, where she has worked since 2024. She has extensive experience in hematologic and solid tumors across diverse populations and has presented at several notable industry conferences.
Work at Asher Bio
Caro U. has been working in Clinical Operations at Asher Biotherapeutics since 2024. In this role, which she has held for five months, she focuses on managing clinical trials and ensuring that operational processes align with the company's objectives. Her responsibilities include integrating patient experiences into trial designs to enhance the relevance of studies.
Previous Experience in Clinical Operations
Before joining Asher Biotherapeutics, Caro U. worked at Kinnate Biopharma Inc. from 2021 to 2024, where she contributed to clinical operations for three years in the San Francisco Bay Area. Prior to that, she spent one year at Telios Pharma, Inc. from 2020 to 2021, and six years at Clovis Oncology from 2014 to 2020, also in the San Francisco Bay Area. Her extensive background includes working with both adult and pediatric populations across various tumor types.
Global Clinical Operations Experience
Caro U. possesses global experience in clinical operations, having worked across multiple regions including North America, Europe, Asia-Pacific (including China and Japan), Africa, and South America. This diverse experience enables her to understand and navigate the complexities of conducting clinical trials in different regulatory environments and cultural contexts.
Conference Presentations and Insights
Caro U. has presented at several prestigious conferences, including SCOPE, Oncology West, OCT, and Proactive GCP. These presentations allowed her to share insights and learn from industry peers, contributing to her professional development and the advancement of clinical practices.
Expertise in Trial Design and Monitoring
Caro U. excels in writing and developing comprehensive plans and processes related to clinical trials. Her expertise includes crafting analytic data review processes and risk-based monitoring plans, which are essential for ensuring the integrity and efficiency of clinical studies.