Ashleigh Willson
About Ashleigh Willson
Ashleigh Willson serves as the Director of Clinical Research at Inari Medical in San Jose, California, where she has worked since 2020. She possesses expertise in core lab management, device accountability, and has a background in clinical trial management and regulatory compliance.
Work at Inari Medical
Ashleigh Willson has been serving as the Director of Clinical Research at Inari Medical since 2020. In this role, she oversees clinical research activities and ensures compliance with regulatory standards. Based in San Jose, California, she has contributed to the development and management of clinical trials, focusing on device accountability and core lab management. Her expertise in clinical research has been instrumental in advancing the company's objectives in the medical device sector.
Education and Expertise
Ashleigh Willson earned a Bachelor of Science degree in Biopsychology from the University of California, Santa Barbara, where she studied from 1998 to 2002. Her educational background provides a strong foundation for her work in clinical research. She possesses specialized skills in developing Case Report Forms (CRF), Source Worksheets, and Electronic Data Capture (EDC) systems, which are essential for managing clinical data effectively.
Previous Experience at EBR Systems, Inc.
Before joining Inari Medical, Ashleigh Willson worked at EBR Systems, Inc. from 2017 to 2020. She held the position of Senior Manager, Clinical Affairs, and later served as Director, Clinical Affairs. During her tenure, she was responsible for overseeing clinical affairs and managing various aspects of clinical trials, contributing to the company's research initiatives in the medical device field.
Clinical Trial Management Experience
Ashleigh Willson has extensive experience in clinical trial management. She worked as a Clinical Trial Manager at Altura Medical Inc. for six months in 2014. Her responsibilities included managing clinical trial operations and ensuring compliance with regulatory requirements. Additionally, she has managed clinicaltrials.gov entries and compliance for clinical studies, demonstrating her proficiency in navigating clinical research regulations.
Skills in Clinical Research
Ashleigh Willson is skilled in managing Investigational Device Exemption (IDE) submissions and generating clinical study reports. Her expertise extends to contract and budget negotiation for clinical trials, which is critical for the successful execution of research projects. Her comprehensive skill set supports her role in advancing clinical research initiatives within the medical device industry.