Jun has over 18 years of experience in the full lifecycle of software development, with 10 years of working and living experience in Japan. He is proficient in Japanese and English, and has dedicated nearly 10 years to the field of pharmacovigilance consulting.

Prior to joining Nextrove, he successively served as a Senior Pharmacovigilance Consultant at IQVIA Japan and IQVIA China. He has led and participated in multiple system implementation and data migration projects for Argus and Argus J. In these projects, he accurately organized requirement workshops, communicated efficiently with clients to deeply explore their needs, and coordinated development work to ensure the efficient delivery of projects.

As a Subject Matter Expert (SME) in this field, he specializes in customized development of E2B/R2/R3 and cross-system data migration (covering systems such as Argus, Argus J, CW5, ArigsG, SoPharma, etc.). He is familiar with drug safety compliance requirements and has an in-depth understanding of the specifications for submitting ICSR (E2B/R2/R3) reports to regulatory authorities including PMDA, FDA, EMA, and NMPA.

In addition, he possesses excellent communication and coordination skills, enabling him to effectively facilitate collaboration among multiple stakeholders such as pharmaceutical clients, software engineers, and partners. Leveraging his bilingual proficiency, he ensures barrier-free cross-team communication.

In terms of educational background, he is currently pursuing a Master of Business Administration (MBA) at Wuhan University, and holds a Master’s degree in Electronic Control Engineering from Wuhan University of Science and Technology. He has dual certifications in Project Management Professional (PMP) and China National Certified Project Manager (CSPM).