Hi everyone! π
I'm So Jin Lee, Pharm.D., Ph.D., Co-Founder/CTO of APLUS Simulation and an Affiliated Professor at Sungkyunkwan University School of Pharmacy, where I teach Clinical Pharmacology and Modeling. My background is in Pharmacometrics, with experience in industry supporting drug development programs across PK/PD, Population PK, PBPK, and translational modeling for IND and NDA/BLA submissions. I'm based in Seoul, Korea, and completed my Pharm.D. at the U of M CoP in Ann Arbor.
More recently, my work has focused on integrating AI/ML with mechanistic modeling to support quantitative decision-making and on building AI/ML-integrated clinical PK/PD prediction software.
I'm excited to join this SIG because I'm enthusiastic about learning from this community and staying up to date with the latest developments. I believe AI/ML should go beyond automating routine tasks-it should enhance scientific reasoning and quantitative decision-making while maintaining transparency and regulatory confidence. I'm particularly interested in AI applications for MIDD, biomarker analysis, translational prediction, and also AI-assisted modeling workflows. Ultimately, I believe the key is not only AI/ML itself, but how PMX-AI/ML experts interpret, validate, and apply AI-generated results/insights to make scientifically sound decisions.
I'm also looking forward to presenting our groups work at ACOP and ISSX this year on AI/ML integration. I hope to meet many of you there! Looking forward to learning from everyone here and exchanging ideas!
(p.s. I would also appreciate it if you could let me know how to remove the photo attachment, if possible. ;) )
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So Jin Lee
Co-founder, CTO / Affil.Prof.
APLUS Simulation / SKKU School of Pharmacy
Seoul
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Original Message:
Sent: 07-01-2026 00:06
From: Euibeom Shin
Subject: Let's Break the Ice! Hi everyone!
Hi everyone!!
I'm Euibeom a PharmD/MS candidate at the University at Buffalo, working with Dr. Murali Ramanathan. My research has been on LLM evaluation for clinical pharmacology, a published paper on LLM assessment of clinical trial protocols (CPT 2025), and I'm currently extending it to first-in-human dose selection. This summer I'm also interning at Lagomorph Technologies on retrieval evaluation for a QSP literature RAG system.
What draws me to this SIG is the evaluation piece specifically the "scores into trust" question of how we go from "the model said X" to "we have enough evaluation rigor to act on X" in high-stakes contexts like dose selection and trial design. (Also recently joined the Agentic Workflows sub-group under this SIG, so nice to see others already here too!) Excited to learn from everyone here and connect.
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Euibeom Shin, M.S.
PharmD Candidate
University at Buffalo
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