Dr. Ming-Hui Chen is
Board of Trustees Distinguished Professor and Head of the
Department of Statistics at the University of Connecticut
(UConn). He was elected to Fellow of International Society for
Bayesian Analysis in 2016, Fellow of the Institute of
Mathematical Statistics in 2007, Fellow of American Statistical
Association in 2005. He also received the University of
Connecticut AAUP Research Excellence Award in 2013, the UConn
College of Liberal Arts and Sciences (CLAS) Excellence in
Research Award in the Physical Sciences Division in 2013, the
University of Connecticut Alumni Association's University Award
for Faculty Excellence in Research and Creativity (Sciences) in
2014, and ICSA Distinguished Achievement Award in 2020. He has
published over 428 statistics and biostatistics methodological
and medical research papers in mainstream statistics,
biostatistics, and medical journals. He has also published five
books including two advanced graduate-level books on Bayesian
survival analysis and Monte Carlo methods in Bayesian
computation. He has supervised or been supervising 37 PhD
students. He served as President of the International Chinese
Statistical Association (ICSA) in 2013, Program Chair and
Publication Officer of SBSS of the American Statistical
Association (ASA) and the ASA Committee on Nomination for
2016-2017 to nominate candidates for ASA President/Vice
President. Currently, he serves as the 2022 JSM Program Chair,
Past President of the New England Statistical Society (nestat.org), Co Editor-in-Chief of Statistics
and Its Interface, inaugurated Co Editor-in-Chief of New England
Journal of Statistics in Data Science, and an Associate Editor
of JASA, JCGS, and LIDA.
Kun Chen is a Professor
in the Department of Statistics at the University of Connecticut
(UConn) and a Research Fellow at the Center for Population
Health, UConn Health Center. He has been a Fellow of the
American Statistical Association (ASA) since 2022 and an Elected
Member of the International Statistical Institute (ISI) since
2016. His research mainly focuses on large-scale multivariate
statistical learning, statistical machine learning, and
healthcare analytics. He has extensive interdisciplinary
research experience in several fields, including ecology,
biology, agriculture, and population health. Dr. Chen has
graduated with over ten PhDs and received Recognition for
Teaching Excellence at UConn multiple times. He has also been
active in professional services. In particular, he was a core
member in establishing the New England Statistical Society
(NESS) in 2017 and served as its secretary until 2021.
Currently, he serves as the Program Chair for the ASA Section on
Statistical Computing and Vice-President for the ASA Connecticut
Chapter.
Dr. Chen received his B.Econ. in Finance and
Dual B.S. in Computer Science & Technology from the
University of Science & Technology of China in 2003, M.S. in
Statistics from the University of Alaska Fairbanks in 2007, and
Ph.D. in Statistics from the University of Iowa in 2011. Before
joining UConn, he was on the faculty of Kansas State University
from 2011 to 2013.
Jeff Palmer has been a
statistics group head leading early clinical development in rare
diseases at Pfizer for the past 5 years. Prior to Pfizer he had
worked for over ten years with various other pharma and
consulting companies supporting mainly rare diseases, oncology,
and neurology. Jeff received his MS in statistics from the
University of Chicago and conducted his doctoral research in
statistics at Carnegie Mellon University.
Dr. Yang Song is
currently Executive Director, Biostatistics Group Head for
Pipeline Development, at Vertex Pharmaceuticals Inc., leading
biostatistics teams supporting multiple rare disease pipeline
development projects. Prior to joining Vertex, he was with Merck
for nearly 10 years, rotated through its PA, Beijing, and NJ
global sites, with increasing responsibilities for global drug
development across multiple therapeutic areas. He also worked
with Johnson & Johnson for oncology drug development early
in his career. His research interests include rare disease
clinical trial methodology, real world evidence, data
integration, optimal clinical development strategy, statistical
issues in oncology clinical trials, biomarker endpoints, and
subgroup analyses. He is a member of the ASA Biopharmaceutical
Scientific Working Group on Real World Evidence. Yang received
his Ph.D. in Statistics from the University of Wisconsin -
Madison.
Dr. Rui (Sammi)
Tang is an innovative, results-oriented pharmaceutical leader
with an established track record of building, launching and
supporting high performing teams, collaborating across
organization lines and developing innovative trials design
options and quantitative solutions that capitalize on
opportunities to produce optimal, cost-effective results. She is
currently the VP, Global Head of Biometrics at Servier
Pharmaceuticals.
Prior to join Servier she was the
Biostatistics Therapeutic Area Head for multiple teams at Shire
Pharmaceuticals including oncology, Transplants, Ophthalmology
and prematurity neonates and has worked at several other
organizations, including Vertex, Amgen, Mayo Clinical and Merck.
At Amgen, she served as the biostatistics lead of Companion
Diagnostics and the Global Statistics Lead for multiple oncology
clinical programs from early phase to late phase. Sammi has
great experience in CDRH, CBER, CDER, health Canada, EMA and
Asian regulatory agencies interactions. Sammi’s research
interests are primarily in the area of adaptive clinical trial
design and biomarker subgroup related statistical issues in
precision medicine. She has authored more than 50 articles in
peer-reviewed scientific journals on methodology, study design,
data analysis and reporting and is a co-inventor of several
patents. Besides her daily work, she actively promotes data
science through many of her volunteer activities: Sammi is
co-founder of DahShu which is a 501(c)(3) non-profit
organization, founded to promote research and education in data
sciences with almost 5000 members internationally. She is
leading teams in the Innovative design scientific working group
(IDSWG) of oncology drug development and small population
working group for rare disease statistical methodology
development. She is also an active member in ASA(American
Statistics Association) and ICSA(International Chinese
Statistics Association) to serve the biostatistics and data
science professional community.
Sammi graduated from
the University of Michigan Technology University with a PhD in
statistics Genetics.
Richard Zhang is the
Statistics Group Lead for late phase clinical development in
rare diseases at Pfizer. He has been in the pharmaceutical
industry for over twenty years with exposure to hundreds of
clinical trials spanning multiple therapeutical areas:
Neuroscience, Pain, Rheumatology, Endocrine and IEM. He has
extensive knowledge and experience in regulatory interactions
and submissions. His research interests include innovative trial
design, real world evidence, meta-analysis, data mining and
modeling. Richard received his PhD in statistics from the
University of Kentucky.
Yingwen Dong is the
Global Head of Biostatistics in Rare Diseases and Rare Blood
Disorders at Sanofi. Prior to this role, she served as the
Deputy Global Head of Oncology Biostatistics in late phase at
Sanofi. She has over 16 years of clinical development experience
in pharmaceutical industry in multiple therapeutic areas
including neurology, oncology, rare diseases and rare blood
disorders. Her research interests are in the area of innovative
clinical trial design and its application. She currently serves
as ICSA representative on 2024 JSM programming committee, and
the steering committee member for 2024 ASA biopharmaceutical
section regulatory-industry statistical workshop. She received
her Ph.D in statistics from University of Minnesota.
HaiYing Wang is an
Associate Professor in the Department of Statistics at the
University of Connecticut. He was an Assistant Professor in
statistics at the University of New Hampshire from 2013 to 2017.
He obtained his Ph.D. from the Department of Statistics at the
University of Missouri in 2013, and his M.S. from the Academy of
Mathematics and Systems Science, Chinese Academy of Sciences in
2006. His research interests include informative subdata
selection for big data, model selection, model averaging,
measurement error models, and semi-parametric regression.
Andy Chi currently serves
as Executive director of Statistics and Quantitative Sciences
(SQS), Data Sciences Institute (DSI) at Takeda. He is a member
of DSI Leadership team (LT) and SQS management team (MT),
supporting development and commercialization of Takeda Oncology
Portfolio. He has 18 years of drug development experience, and
has been strong advocate for innovative trial design and
quantitative decision making using diverse trial types and data
sources in clinical trials, from Academia and RWD/RWE. Andy
received his MS in biometry from University of Texas, Houston,
and PhD in Medical Science from University of South Florida.
Ran Duan is currently the
Director of biostatistics at Vertex Pharmaceuticals oversee
multiple indications. Before join Vertex, Ran worked at Angitia,
Alexion, AstraZeneca Rare Disease and Eli Lilly and Company,
where she supported the clinical development in multiple
therapeutic areas including Bone disease, neurology,
ophthalmology, and diabetes programs. She is an active member of
the ASA Gene and Cell therapy working group. Her research
interests include the innovative trial design for gene and cell
therapy, rare disease, RWE generation and digital solutions for
health care.
Dr. Roee Gutman is a
Professor in the Department of Biostatistics at Brown
University. His areas of expertise are causal inference, file
linkage in the absence of unique identifiers, missing data,
Bayesian data analysis and their application to big data sources
in health services research. He has vast experience in analysing
many types of secondary datasets from various sources (e.g.
Medicare claims data, registries, VA health data), as well as
data collected through large pragmatic randomized trials. Dr.
Gutman has been the principal investigator of multiple NSF, NIH
and PCORI grants and is the lead statistician on NIH, PCORI and
VA grants. Recently, he received ISPOR Health Economics Outcomes
and Research - Methodology Award and he was ASA/NSF/BLS Senior
Research Fellow.
Dr. Li currently holds the
position of Principal Clinical Data Scientist at Boehringer
Ingelheim. In her current role, Dr. Li leads a Biostatistics and
Data Science development team as the Product Owner for clinical
portfolios developed for rare disease indications in
inflammation. Dr. Li's academic credentials include a Master of
Science (M.S.) and a Doctorate (Ph.D.) in Statistics, both
earned from the University of Connecticut, Storrs. She achieved
these degrees in December 2017 and August 2018, respectively.
Beyond her work at Boehringer Ingelheim, Dr. Li actively
contributes to the broader scientific community by serving as a
reviewer for several academic journals and extending her work to
publications.
PhD in Biostatistics, Sr.
director of biostatistics, rare disease TA leader in Moderna
with enriched 18 years’ experience in biopharmaceutical industry
for clinical trial design, study implementation, NDA/BLA
submission, and regulatory interaction across multiple TAs.
Dr. Susie Sinks is
currently a Director in Development Statistics at Biogen, where
she has served as program lead in neuromuscular, multiple
sclerosis and immunology therapeutic areas. Before joining
Biogen in 2019, Susie worked in the FDA over 5 years for the
Division of Metabolic and Endocrinology Products (DMEP) with
specialty in diabetes and metabolic statistical review after
receiving a Ph.D. in Biostatistics from Virginia Commonwealth
University. Her research interests include missing data,
surrogacy modeling, benefit and risk assessment.
Dr. Lin Wang currently serves
as the Vice President and Head of Biometrics at Insmed. Prior to
joining Insmed, She spent more than 17 years at Sanofi where she
held positions of increasing responsibility, including as Global
Biostatistics Head for Rare Diseases and Rare Blood Disorders.
Lin has extensive clinical development experience in all stage
of clinical development from pre-IND, global NDA/MAA submissions
to approvals across multiple diseases for small, large molecules
and gene therapies. Her research interests include rare disease
clinical trial design and analysis methodology, count data,
adaptive design. Lin earned her Ph.D. in Statistics from the
University of Wisconsin-Madison.
Dr. Xin Wang is Senior
Director in BMS leading Cell Therapy Breyanzi Franchise
Biometrics Team. Xin received her Ph.D in Statistics from
Northwestern University, since then she has 16+ years of
experience in pharmaceutical industry. Prior to joining BMS in
2021, Xin was TA Lead of Rheumatology at AbbVie where she held
positions with increasing responsibilities with 5 years as
people manager. Xin has led the Rheumatology statistics team
with significant contributions to the submission and approval of
Rheumatology indications in Rinvoq and Humira. Prior to AbbVie,
Xin had worked at Pfizer and Sanofi in Inflammation, CVMED and
internal medicine. Her research interest includes multiple
comparisons, gatekeeping procedures, dose-finding, missing data
imputations, and adaptive designs.