Yoshi is a seasoned business development professional with over 10 years of experience in the clinical research industry. He led strategic partnerships with biotech, pharmaceutical, and medtech sponsors, providing tailored CRO solutions that support clinical trials across all phases in compliance with ICH-GCP and regional regulatory requirements. Yoshi has extensive experience in both drug and medical device development, with a strong focus on trials in oncology, rare diseases, and cardiovascular indications. He also has deep expertise in the regulatory landscape in the Asia-Pacific (APAC) region, including Japan, South Korea, Australia, and Singapore—advising clients on study planning, regulatory submissions, and regional trial optimization. A frequent attendee at key industry events, Yoshi actively engages with global innovators at the J.P. Morgan Healthcare Conference, BIO International Convention, and the DIA Global Annual Meeting, helping to shape forward-thinking partnerships and stay at the forefront of clinical development trends.