SiewTin Gan
Vice President, Head of Clinical Operations and Data Management Acumen Pharmaceuticals
Siew Tin Gan is a clinical research professional with more than 20 years of progressive experience in the clinical research and drug development primarily in CNS indications, serving various leadership roles in clinical operations and project management.
Prior to joining Acumen in November 2021, Gan was at Takeda Pharmaceutical for three years overseeing several key clinical programs in neuroscience. Before relocating to the US, she was at Lundbeck for 11 years where she was instrumental in the growth and establishment of the Lundbeck Clinical Development Center located in Singapore. Following that, Gan joined Danone Nutricia Research and led a cross-functional study execution team in early life nutrition research for three years.
Gan received a Bachelor of Science in chemistry and biochemistry from the National University of Singapore and a Master of Science in nutritional science from the University of Sydney.
Seminars
This hands-on workshop moves beyond theory and puts attendees in the role of trial designers. Working in small groups, participants will deconstruct real-world protocols, identify recruitment risks, and collaboratively redesign studies to improve feasibility, patient experience, and enrollment outcomes. By the end of the session, attendees will leave with practical tools and frameworks that can be immediately applied to future studies.
Attend this workshop to:
- Stress-test protocol designs through guided group exercises and identify hidden barriers to recruitment and retention
- Balance scientific objectives with operational feasibility and participant burden when making design decisions
- Build a practical framework for designing studies that patients can join, sites can execute, and sponsors can successfully recruit into
