The PharmaDS 2025 Organizing Committee comprises industry leaders, academics, agency members, and professionals dedicated to advancing the future of pharmaceutical data science.
Our legacy members have played a pivotal role in shaping the PharmaDS conference over the years, contributing their vision, leadership, and expertise to its enduring success.
This year, our non-legacy members further diversify the committee expertise to ensure PharmaDS continues shaping the future of pharmaceutical data science.
Rebecca Taha, PhD, MBA, CEO &
Founder of waterworksAI, is a strategic leader in the life
sciences industry. With a deep understanding of both
scientific research and business operations, Dr. Taha guides
waterworksAI in the delivery of innovative, technology-based
solutions that address critical challenges in drug
development. With over 20 years of experience in the
industry, she has a proven track record of delivering
impactful solutions. Prior to founding waterworksAI, Dr.
Taha served small, medium, and large pharma and biotech
organizations in the strategic development and
implementation of their clinical development programs. Dr.
Taha received her MS and PhD from the University of Kentucky
in Statistics and Gerontology, respectively, and her MBA
from the Kelley School of Business.
Dr. Jingjing Ye is an executive
director and currently leads a global team, Data Science and
Digital Innovations (DSDI), with Global Statistics and Data
Sciences (GSDS) in BeiGene. She has over 17 years’
experience in pharmaceutical industry and US FDA, with focus
in cancer drug discovery and development. Her statistical
and regulatory experience expands full spectrum on patients’
treatment journey from diagnosis, treatment, to living with
the condition. She is very active in statistical communities
in US and between US and China DIA communities, including
leading several cross-disciplinary and cross-company working
groups. She received her PhD degree in statistics from
University of California, Davis and BS in applied
mathematics from Peking University.
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.
With 18 years in the
pharmaceutical industry, Pritibha focuses on solving complex
global business challenges by integrating analytics,
development strategy, and stakeholder alignment to deliver
outcomes. Pritibha’s Statistics and Program Management
leadership in cross-functional teams has driven insights,
operational efficiency, and sustainable growth.
Leveraging her unique blend of psychology, statistics, and business expertise, I translate intricate data-driven insights into impactful strategies. Her sustainability doctoral research on decentralized clinical trials at ETH Zurich reflects her commitment to innovation and human-centric solutions. Passionate about driving strategic transformation, she fosters collaboration, inspires change, and delivers results in dynamic, high-stakes environments. She has an MBA from the University of St Gallen (Switzerland) and from the University of Auckland (New Zealand), her MSc in Medical Statistics, a Post-Graduate Diploma in Statistics, and a Bachelor of Science in Psychology and Statistics.
Dr. Joan Buenconsejo is the
Vice President and head of Cardiovascular and Neuroscience
Biostatistics at Bristol-Myers Squibb. In addition to
leading a team of talented statisticians who support the
development of innovative therapies for patients with CV and
neurological diseases, she is also co-leading a BMS-wide
workstream that aims to foster trial design innovation and
optimization. Dr. Buenconsejo has over 20 years of drug
development experience, having worked at the Food and Drug
Administration and AstraZeneca before joining BMS. While she
calls statistics as her “bread and butter” skillset, she is
also passionate about applying novel tools and technology to
generate insights, simplify workflows, and reduce patient
burden in clinical research. She is also an advocate of
using innovative trial designs to accelerate the development
of promising new therapies. Dr. Buenconsejo holds a Ph.D.
and an MPH in Biostatistics from Yale University.
Numan Karim is an Associate Director of
Data Science & Analytics at AbbVie. He has 8 years of
experience in the pharmaceutical industry, with a focus on
enabling analytics capabilities across Clinical Development,
with an emphasis on Patient Safety analytics.
Numan's current work involves developing fit-for-purpose
analytics platforms for healthcare professionals and
scientists to easily navigate, interrogate, and survey
complex clinical data to ensure patient safety and the
safety of AbbVie drugs. Combining visual analytics,
statistics, and modern data engineering tactics, he has
deployed multiple data science products at scale, enabling
patient safety insights and surveillance in an automated,
self-service manner. Numan is passionate about data science
leadership and the intersection of analytics, technology,
and medicine.
Numan received a B.S. in Statistics
& Integrative Biology from the University of Illinois at
Urbana Champaign in 2016, and received a M.S. in Applied
Data Science from the University of Chicago in 2020.
Wei Zhong is a Senior Director of
Biostatistics at BioNTech SE and providing strategic
guidance into oncology drug development and regulatory plan.
He has over 12 years’ in-depth experience in phase I-IV
clinical trials with the focus on oncology and CNS in big
pharma companies including Genentech, Takeda and Pfizer. Wei
is a recognized expert in innovative trial designs, Bayesian
methodology, and pharmacometrics, with a solid publication
record (30+ papers). Wei is playing an active role in
scientific community and professional society as Conference
Organizer, Session Chair and Invited Speaker in national
statistical conferences. He is currently the VP of New
England Statistical Society to lead NextGen Committee to
support the next generation of statisticians and data
scientists. Wei received his PhD in biostatistics and MS in
pharmacometrics from University of Minnesota and BS in
biotechnology from Shanghai Jiao Tong University.
Sofia Fleyshman is a Principal
Scientist in Clinical Safety Statistics at Merck supporting.
She has over 14 years of experience in pharmaceutical and
medical devices industries in small, mid-size, and large
pharma companies and CRO. Her current interests are in
exploring how AI can be used to streamline pharmaceutical
work. Sofia received her MS and BS in Mathematics with
Concentration in Statistics from University of
Massachusetts, Amherst.
Philip He is Head of Statistical Strategy, Innovation and
Safety at Daiichi Sankyo. He has extensive experiences in
pharmaceutical industry. Philip received his PhD in
biostatistics from University of Minnesota, Twin Cities. His
current role focuses on developing and implementing
statistical and data science solutions for drug development
including innovative study designs, safety methodology and
data science.
Chenchen Wang is a Principal Data
Scientist at Amgen. She has 4 years’ experience in
pharmaceutical industry, with focus in developing predictive
models for site selection and building AI platforms to
support clinical research. Chenchen received her PhD in
Computational Materials Science from University of
Connecticut and MS in Computer Science from Georgia
Institute of Technology. Her current work focuses on
harnessing AI to optimize clinical trials and streamline
research processes.
Ping Li is a statistical analyst in the
Division of Analytics and Informatics (DAI), Office of
Biostatistics (OB) at CDER/FDA. Her primary duty is to
support statistical reviews of IND/NDA/BLA applications in
collaboration with all Divisions of Biometrics in OB. She
co-leads the DAI Bayesian Working Group and is a member of
the OB’s Missing Data Working Group and Subgroup Analysis
Working Group. Additionally, she has been involved with the
standardization of programs for data analysis, a project
supporting computational and programming needs, and
strengthening efforts to standardize processes across OB
divisions. She received her MS in Biostatistics and
Epidemiology from Georgetown University.
Rebecca Vislay-Wade, PhD is a
Senior Principal Data Scientist at Moderna, where she leads
a team of scientists developing AI applications for clinical
operations, regulatory science, and pharmacovigilance. Prior
to Moderna, she worked as Senior Research Data Scientist at
Highmark Health. Rebecca holds a PhD in biochemistry from
Harvard University and did postdoctoral work in neuroscience
at the NIH and Children’s National Medical Center in
Washington, DC. She currently lives in the Boston area with
her family.
Dr. Zhan(Harold) Ye is currently
the associate director of non-clinical biostatistician at
Pfizer Inc. for Digital Genomics Precision Medicine
Statistics. He received his PhD in Mathematics, focusing on
statistical genetics from Michigan Technological University,
and then worked as senior biostatistician for Marshfield
Clinical Research Foundation before joining Pfizer in
2017.