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Meet the Program Commitee for 2023!
Program Committee
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Venkatraman Balasubramanian, PhD, MBA
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Healthcare and Life Sciences Strategic Advisor
VB Insights, LLC, United States -
Greg Ball, PhD
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Safety Data Scientist
ASAPprocess, United States -
Amy Bertha
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Executive Director, Regulatory Policy and Science
Bayer, United States -
Claire Blanchette, PMP
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Executive Drug Development Program Leader
Consultant, United States -
Susan Callery-D'Amico, BSN
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Retired, Vice President, R&D Quality Assurance, AbbVie
United States -
Brooke Casselberry, MS, RAC
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Vice President, Advisory and Delivery
Epista Life Sciences, United States -
Meghana Chalasani, MHA
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Associate Director for Clinical Trial Innovation, Office of New Drugs, CDER
FDA, United States -
Andrew Chang, PhD
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Vice President, Quality and Regulatory Compliance
Novo Nordisk, United States -
Wendy Charles, PhD
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Chief Ethics and Compliance Officer; Adjunct Faculty
Equideum Health, United States -
Ethan Chen, MBA, MS, PMP
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Director, Division of Data Management Services and Solutions, OBI, OSP, CDER
FDA, United States -
Leah Christl, PhD
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Exec Director, Global Biosimilars Regulatory Affairs & Regulatory & R&D Policy
Amgen, United States -
Mary Ellen Cosenza, PhD, MS, RAC
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President
MEC Regulatory & Toxicology Consulting, LLC, United States -
Stephanie Y. Crawford, PhD, MPH, MS
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Professor, Pharmacy Systems, Outcomes and Policy
University of Illinois at Chicago, United States -
Alysha Croker, PhD
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Director, Centre for Policy, Pediatrics and International Collaboration, BRDD
Health Canada, Canada -
Ebony Dashiell-Aje, PhD
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Executive Director and Head, Patient Centered Outcomes Science
BioMarin, United States -
Julie Dietrich, MS
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Vice President, Clinical Development
GENFIT, United States -
Andrew Emmett, MPH
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FDA Liaison | US Regulatory Policy and Global Intelligence
Pfizer Inc, United States -
Jennifer Farmer, MS
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Chief Executive Officer
Friedreich's Ataxia Research Alliance (FARA), United States -
Maureen Feeney, PharmD, MBA, RPh
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Vice President Scientific Communications and Strategic Alliances
Takeda, United States -
Ron Fitzmartin, PhD, MBA
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Senior Advisor, Office of Regulatory Operations, CBER
FDA, United States -
David Fryrear, MS
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Executive Vice President and Head of Quality Assurance
Astellas, United States -
M. Scott Furness, PhD
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Deputy Director, Office of New Drug Products, OPQ, CDER
FDA, United States -
Alicia Gilsenan, PhD, MS, RPh, FISPE
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Vice President, Epidemiology
RTI Health Solutions, United States -
Cheryl Grandinetti, PharmD
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Associate Director for Clinical Policy, CDER/OC/OSI/DCCE
FDA, United States -
Renmeet Grewal, PharmD, MS
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Division Director, Office of Regulatory Operations (DRO-II), OND, CDER
FDA, United States -
Sabine Haubenreisser, PhD, MSc
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Principal Scientific Administrator, Stakeholders and Communication Division
European Medicines Agency, Netherlands -
Alan Hochberg
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Principal Scientific Enablement Director, Scientific Enablement and Processes
Genentech, A Member of the Roche Group, United States -
Michelle Hoiseth
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General Manager, Project-Based Services
Cytel, United States -
Cammilla Horta Gomes, MA, MPharm
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Latam Regulatory Policy Lead
Roche, Brazil -
Emily (Xianghong) Jing, PhD
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Associate Director for Scientific Coordination, OBP, OPQ, CDER
FDA, United States -
Jeremy Jokinen, PhD, MS
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Vice President and Head, Safety Evidence and Sciences
Bristol-Myers Squibb Company, United States -
Cathryn C Lee, MSN
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Director, Office of Program Operations, PDIMS, OND, CDER
FDA, United States -
Demetra Macheras, MBA
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Director, Regulatory Policy and Intelligence - Regulatory Affairs
AbbVie, United States -
Nicole Mahoney, PhD
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Executive Director US Regulatory Policy & Intelligence
Novartis Pharmaceuticals Corporation, United States -
Sheila Mahoney Jewels, MBA
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Drug Development Multi-Functionalist
LifeSciHub , United States -
Ingrid Markovic, PhD
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Senior Science Advisor for CMC, Office of the Center Director, CBER
FDA, United States -
Lindsay McNair, MD, MPH, MS
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Principal Consultant
Equipoise Consulting, United States -
Melodi J McNeil, MS, RPh
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Director, Regulatory Policy and Intelligence
AbbVie, United States -
David Meats
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Director, Regulatory Services Management
Certara, United States -
Munish Mehra, PhD, MS, MSc
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Managing Director and Sr. Principal Biostatistician
Quantum Biopharma, United States -
Timothe Menard, PharmD, MSc
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Global Head, Quality Excellence Digital | Bioethics Coach (Data Ethics)
F. Hoffmann-La Roche Ltd, Switzerland -
Alexis Miller, JD
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Acting Global Lead, Global Regulatory Policy and Intelligence
Merck & Co., Inc., United States -
Martha Monser
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Consumer Safety Officer, Office of Regulatory Operations, CBER
FDA, United States -
Christine Moore, PhD
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Executive Director, Global External Advocacy and Standards
Organon & Co., United States -
Erin Mulrooney, MSc, PMP
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Director, Portfolio Management
Daiichi Sankyo, Inc, United States -
Sissi Pham, PharmD
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Chief Executive Officer
AESARA, United States -
Margaret Richards, PhD, MPH
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Executive Director, Solutions
Panalgo, United States -
Cynthia Rothblum-Oviatt
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Science Policy Analyst, Rare Disease Team, OND, CDER
FDA, United States -
Leslie Sam
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President
Leslie Sam and Associates, LLC, United States -
Earl Seltzer, MBA
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Senior Director, Partnerships and Innovation
CTI, United States -
Anjali Shah, PharmD
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Executive Director, Business Capabilities and Innovation, WWPS
Bristol-Myers Squibb Company, United States -
Elizabeth Somers, MS
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Executive Director, Global Project and Alliance Management
Merck Sharp & Dohme LLC, United States -
Mat Soukup, PhD
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Deputy Director, Division of Biometrics VII, OB, OTS CDER
FDA, United States -
Shannon Sparklin, MS
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Project Manager, OPPD, OMP, CDER
FDA, United States -
Ling Su, PhD
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Research Fellow
Shenyang Pharmaceutical University, Yeehong Business School, China -
Linda B Sullivan, MBA
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Senior Fellow
Tufts Center For the Study of Drug Development, United States -
Phil Tregunno
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Deputy Director - Patient Safety Monitoring
Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom -
Pujita Vaidya, MPH
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North America Lead, Regulatory Science and Policy
Sanofi, United States -
Paula Walker, MA
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Global Head of Risk Based Quality Management
Roche Products Ltd., United Kingdom -
Susan Wang, PhD
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Global Head of Biostatistics and Data Sciences Inflammation
Boehringer Ingelheim, United States -
Nancy Watanabe, MS, PMP
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Independent Consultant
Independent Consultant, United States -
Keith Wenzel
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Volunteer
DIA Study Endpoints Community, United States -
Jennifer Whiteley, PhD, MSc
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Executive Director, Head OMNI Evidence for Access
Genentech, A Member of the Roche Group, United States -
Robin Whitsell
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President
Whitsell Innovations, Inc., United States -
Judith Zander, MD
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Director, Office of Pharmacovigilance and Epidemiology, OSE, CDER
FDA , United States -
Martine Zimmermann, PharmD
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Senior Vice President, Head of Global Regulatory Affairs
Ipsen , France