DIA 2024 Global Annual Meeting: Full Schedule

12:15pm PDT

#POS 1: Professional and Student Poster Session 1

Component Type: Session

Professional and Student Posters provide an opportunity for methodology (“how to”), case study, and research to be presented to a diverse group of scientific professionals who are actively involved in the discovery, development, and lifecycle management of pharmaceuticals, biotechnology, medical devices, and healthcare-related products.

Speakers

Ilyoung Ahn

Scientific Officer, Institute of Food and Drug Safety Evaluation, Korea, Republic of

Salman Alharthi

Head of Formulary Management, Security Forces Hospital, Saudi Arabia

Ashwin Anand

Engagement Manager, Forian, United States

Jorge Azar

Senior Area Regulatory Director for Latin America, AstraZeneca, United States

Jorge Azar is currently Senior Area Regulatory Director for Latin America with 25 years’ experience on different roles at local, regional and global level in the Regulatory Affairs field, including product strategy, regulatory policy and intelligence. Jorge earned a degree in Pharmacy... Read More →

Jan-Georg Bohlken

Student, University of Bremen, Germany

I studied biology at the University of Göttingen, with a focus on bioinformatics. While working at the Max-Planck Institute for Experimental Medicine, I discovered my interest in statistics. In April of 2024, I finished my Masters in biostatistics. During an industry internship in... Read More →

Paul Bolot

Global Regulatory Strategist, Bayer Consumer Care AG, Switzerland

Paul Bolot is a PharmD by training, with a Master's degree in International Drug Registration and Development. He worked as a regulatory consultant at PharmaLex for three years. Since 2021, he works at Bayer as Global Regulatory Strategist. His work focuses on Regulatory Science... Read More →

Tuiana Brown

PharmD Candidate 2025, Chicago State University, United States

My name is Tuiana Brown, a PharmD Candidate (2025) at Chicago State University College of Pharmacy. During my tenure at Chicago State, I began to appreciate research very much. I completed three years of research with the RISE, CAHMPS, and SRTP programs. I also completed an internship... Read More →

James Browning

Director of Biostatistical Programming, Center for Observational Research, Amgen, United States

James Browning, MPH, is a Director of Biostatistical Programming in the Center for Observational Research (CfOR) at Amgen Inc. He has over 15 years of experience conducting observational studies in multiple therapeutic areas with the majority concentrated in oncology. He is skilled... Read More →

Xianwen Chen

student, University of Macau, Macao

Chen Xianwen is currently a PhD candidate in the Institute of Chinese Medical Sciences at the University of Macau. Her research interests include drug regulatory science and drug policy. In 2020–2022 she obtained her Master’s degree at University of Macau, then she worked as an... Read More →

Joan Cheung

Senior Consultant, NNIT, United States

Joan Cheung received her Doctor of Pharmacy degree from St. John's University and has been recognized by her colleagues in developing a labeling solution with a Product Excellence Award in 2022. She leverages her pharmacy background and technical acumen as a Business Analyst and Project... Read More →

Constance Chisha

PhD Student, University of the Witswatersrand, South Africa

Constance Sakala Chisha is a doctoral candidate pursuing a PhD at the University of the Witwatersrand. She holds a Bachelor’s degree in Pharmacy from the University of Zambia and a Master’s degree in Pharmaceutical Services and Medicines Control from the University of Bradford... Read More →

Grace Collins

Regulatory Policy Analyst, Friends of Cancer Research, United States

Grace Collins is a regulatory policy analyst at Friends of Cancer Research where she conducts research to support the organization’s science, policy, and patient advocacy initiatives. In her role, she leads the creation of public data dashboards for assessing trends in oncology... Read More →

Sahith Doppalapudi

Sr. Manager, PV Analytics Center of Excellence, Bristol-Myers Squibb Company, United States

Sahith Doppalapudi holds a master's degree in Chemical Engineering from Oklahoma State University and has accumulated over 14 years of experience in the pharmaceutical industry. Throughout his career, he has served in different roles including Quality Analyst, Validation Lead, and... Read More →

Christopher Doyle

Senior Director, IBC Services, WCG, United States

Chris is Sr. Director of IBC Services at WCG, where he works with clinical trial stakeholders to ensure research involving gene-based medicines is conducted safely and efficiently. Chris received his PhD in Molecular Genetics and Microbiology from Stony Brook University in 2014. Prior... Read More →

Nora Emmott

Senior Policy Analyst, Duke Margolis Institute For Health Policy, United States

Nora Emmott is the Senior Policy Analyst for the Real-World Evidence Collaborative at Duke-Margolis Center for Health Policy where she works on projects related to patient-generated health data, pharmacogenomics, and precision medicine. She has an MPH with a concentration in Health... Read More →

Jeanine Flanigan

HEOR specialist, Sandoz, United States

Jeanine Flanigan is a HEOR Specialist at Sandoz. She is a graduate of the University of Pittsburgh School of Pharmacy (PharmD '21 and MS '23) and completed a fellowship with Pitt Pharmacy & Sandoz in pharmacoanalytics and outcomes research.

Kayla Garvin

Sr Regulatory Health Project Manager, FDA, United States

I am a Senior Regulatory Health Project Manager with FDA/CDER’s Office of Medical Policy (OMP). I have an MPH from the University of New England and have been with the Agency for 19 years and with OMP for 15 years. I coordinate the workflow for various cross-Agency programs, including... Read More →

Neda Gharavi

Senior Director Medical Writing & Regulatory Affairs, BioPharma Services, Canada

Dr. Gharavi's career in the pharmaceutical industry has been defined by her unwavering passion for science. With a Pharm D degree and a PhD in Drug Metabolism, she has made significant contributions to pharmaceutical industry. Starting as a Pharmacokinetic Scientist at Apotex, she... Read More →

Tapash Ghosh

TL, FDA, United States

Nick Henscheid

Senior Scientist, Critical Path Institute, United States

Nick Henscheid completed his PhD in Applied Mathematics in 2018 with a focus on image science and precision medicine. Since 2021 he has worked for the Critical Path Institute developing advanced quantitative modeling solutions for a variety of needs across the drug development li... Read More →

Li Huang

Principal Biostatistician, Phastar, United States

Li Huang is a principal biostatistician in PHASTAR since 2020. She received Doctor of Dental Surgery (DDS) from Hubei Medical University (China), Master of Science in Dentistry from National University of Singapore (NUS), and Master of Science in Applied Statistics from California... Read More →

Toshiko Ishibashi

Oncology Medical Science Department, Medical Affairs Division, Daiichi Sankyo Co., Ltd., Japan

Toshiko Ishibashi is an Associate Director of Oncology Medical Science in Medical Affairs at Daiichi Sankyo Co., LTD. since 2020. She served Ono Pharmaceutical Company from 2018 to 2020. She was a Clinical Operations Manager at Abbvie, 2016-2018. She has experience as an assistant... Read More →

Rajashekhar Ittedi

Student, Northeastern University, United States

I am a motivated and aspiring regulatory affairs professional with a strong pharmacy background and clinical research skills. Currently, I am pursuing my Master's degree in Regulatory Affairs for Drugs, Biologics, and Medical Devices at Northeastern University, where I am gaining... Read More →

Zarnab Jillani

Medication Error Pharmacovigilance and Risk Management Fellow, FDA, United States

James Kim

Undergraduate Student Researcher, University of Southern California, United States

James is a rising junior studying Neuroscience at the University of Southern California. He is an undergraduate student researcher in the Regulatory Science Team and is studying the use of patient-reported outcome measures in clinical trials for Parkinson's Disease. At school, James... Read More →

Yueh-Wen Lan

Senior Project Manager, Center for Drug Evaluation, Taiwan

Yueh-Wen Lan, a senior project manager in the Division of Regulatory Affairs and Compliance at CDE Taiwan for more than 6 years, has participated in project management for reviewing cases of clinical trials, generic drug registration, and new drug registration. I hold a Master's Degree... Read More →

Juan Lara

Senior Research Analyst, Centre For Innovation In Regulatory Science, Mexico

Juan is a Senior Research Analyst at the Center for Innovation in Regulatory Science. He holds a Bachelor's degree in Pharmaceutical-Biological Chemistry and has diverse experience in quality assurance, production, R&D, and regulatory affairs. Juan supports a wide range of regulatory... Read More →

Liyang Lyu

Student, University of Macau, Macao

Liyang Lyu, a PhD candidate at the University of Macau, specializes in pharmaceutical patent research, with a primary focus on cancer immunotherapy. She has authored two articles in Nature Biotechnology, focusing on the advancements in iPSC and CAR-T therapies.

Jessica Miller

1st-Year Fellow, Global Regulatory Affairs CMC, GlaxoSmithKline, United States

Namosha Mohite

Assistant Director, Global Regulatory Affairs, Bayer, United States

Namosha Mohite, PharmD, is a Manager in the Global Regulatory Affairs group at Bayer. In her current role, she serves as a US regulatory strategist for a product in late-stage development and also supports related global regulatory activities. Her background in pharmacy and interest... Read More →

Nancy Ngum

Student, University of Hertfordshire, United Kingdom

Nancy Yang-Ngum is currently a Doctoral student with the University of Hertfordshire in the United Kingdom. Her research in regulatory science is focused on an assessment of the Regulatory Review Systems in the East Africa Community (EAC) with a view to improving Patients’ Access... Read More →

Bridget Nugent

Science Policy Analyst, FDA, United States

Bridget Nugent, PhD, is a Science Policy Analyst who leads regulatory science initiatives for FDA CDER’s Rare Diseases Team (RDT). Dr. Nugent is a neuroscientist with over 16 years of research and mentorship experience with expertise in rare disease drug development, molecular biology... Read More →

Ashley Ogawa-Wong

Medical Writer, Merck Sharp & Dohme LLC, United States

Ashley is a senior medical writer at Merck & Co., Inc. Since joining medical writing in 2020, Ashley has supported several successful filings to worldwide regulatory agencies. She has authored clinical trial protocols, briefing packages, Investigator’s Brochures, Clinical Study... Read More →

Mercy Owusu-Asante

Graduate Student, School of Life and Medical Sciences, University of Hertfordshire, United Kingdom

Mrs Mercy Owusu-Asante is a pharmacist with an MSc in Pharmaceutical Services and Medicines Control obtained from the University of Bradford, UK. In the area of personal professional development, Mercy is pursuing a PhD in Regulatory Science at the University of Herfordshire, UK... Read More →

Sydney Ringold

Customer Success Manager, Cytel, Inc., United States

Sydney Ringold is a Customer Success Manager at Cytel. She has a diverse background, having received her B.S. in biology and MBA in operations management from the University of Alabama. She has experience in both commercial and research aspects of clinical trials through cofounding... Read More →

Bhavana Tallavajhula

Director, Bristol Myers Squibb, United States

Bhavana Tallavajhula is a highly accomplished pharmaceutical professional with over 20 years of experience at Bristol Myers Squibb (BMS). She began her career as a Formulation Scientist, gaining expertise in laboratory work. Driven by a desire to make a tangible impact on patient... Read More →

Jacqueline Vanderpuye-Orgle

Vice President, Parexel, United States

Shruti Vig

Graduate Student, University of Maryland, College Park, United States

Shruti Vig is a fifth-year Ph.D. candidate in the Department of Bioengineering at the University of Maryland. Currently under the mentorship of Dr. Huang Chiao Huang and Dr. Graeme F. Woodworth, her research focuses on developing test methodologies for evaluating the phototoxicity... Read More →

Stuart Walker

Professor and Consultant, Centre for Innovation In Regulatory Science (CIRS), United Kingdom

Professor Stuart Walker, BSC, PhD (London), MFPM, FRSC, FiBiol, FRCPath, is an independent Consultant in Pharmaceutical Medicine and Founder of both the Centre for Medicines Research (CMR) International and the Centre for Innovation in Regulatory Science (CIRS). UK

Felix Yang

US Regulatory Policy Fellow, Genentech, A Member of the Roche Group, United States

Felix Yang, PharmD, is a US Regulatory Policy Post-Doctoral Fellow at Genentech, a member of the Roche Group in conjunction with Howard University. Felix obtained his PharmD from the University of Wisconsin-Madison. During his first year at Roche-Genentech, he has conducted projects... Read More →

Scarlett Yang

Senior Regulatory Affairs Associate, Gilead Sciences, United States

Scarlett Yang is a Senior Regulatory Affairs Associate at Gilead and supports various regulatory intelligence and policy activities. Scarlett brings partners and stakeholders together across sectors to tackle challenges in drug development. Scarlett holds a PhD in Immunology from... Read More →

Jiewei Zeng

Associate Director, Abbvie, United States

Dr. Jiewei Zeng is an Associate Director at AbbVie. She had Ph.D. in mathematics with a major in statistics from the University of Illinois at Chicago, where her research focused on developing optimal designs for compartment models. Dr. Zeng has extensive experience working in the... Read More →

Monday June 17, 2024 12:15pm - 2:15pm PDT
Posters Exhibit Hall San Diego Convention Center 111 W Harbor Drive, San Diego, CA 92101 USA

18: Posters, Session

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11:15am PDT

#POS 2: Professional Poster Session 2

Speakers

Malak Almutairi

Researcher, Saudi Food and Drug Authority, Saudi Arabia

I am a researcher specialized in regulatory research with a master's degree in pharmacy and Pharmaceutical Sciences. I have been working in the SFDA (Saudi Food and Drug Authority) for several years now, and my focus has been on ensuring the safety and efficacy of pharmaceutical products... Read More →

Daniel Alvarez

Principal Medical Director, Health Equity and Inclusive Research (HEIR), Genentech, A Member of the Roche Group, United States

Dr. Daniel Alvarez earned his medical degree from the Institute of Medical Science of Havana, Cuba in 2002 and the University of Costa Rica in 2006. He also holds a master's degree in Science of Pharmaceutical Medicine from Hibernia College, Ireland, in 2016 and a Diploma in Pharmacoeconomics... Read More →

Celeste Amadei

Product Manager, PAK Biosolutions, United States

Cheng Chi Chen

Clinical Reviewer, Center For Drug Evaluation, Taiwan

Cheng Chi Chen, Clinical Reviewer, Division of New Drugs, CDE, Taiwan Cheng Chi Chen has been a Clinical Reviewer in Division of New Drugs at CDE Taiwan for more than 1 years. Cheng Chi Chen is a Pharmacist and holds a Master’s degree in Clinical Pharmacy from National Yang Ming... Read More →

Renata Costa

Specialist, LIBBS FARMACEUTICA, Brazil

Renata Watanabe Costa has a degree in Biomedicine, with a postgraduate degree in Research and Development of Medicines and a Master's in Sciences from the Federal University of Sao Paulo (Brazil). She has 13 years of experience in the pharmaceutical industry in the areas of Medical... Read More →

Samantha Cotter

Safety Evaluator, FDA, United States

Dr. Samantha Cotter is a pharmacist and safety evaluator in the Division of Pharmacovigilance within the Office of Surveillance and Epidemiology at the US Food and Drug Administration (FDA). Samantha has over 20 years of clinical pharmacy experience, and 12 years in research at the... Read More →

Matt D'Ambrosio

Policy Analyst, Duke-Margolis Institute For Health Policy, United States

Matt D'Ambrosio is a policy analyst with the Duke-Margolis Institute for Health Policy's Biomedical Innovation portfolio. He primarily works with the Institute's Real-World Evidence Collaborative--providing support on workstream deliverables and stakeholder engagement. Matt is based... Read More →

Tiffany Dominic

Risk Management Fellow, Pfizer, United States

Tiffany Dominic is a Post-Doctoral Risk Management Fellow at Pfizer, in conjunction with Rutgers University. She graduated with her Doctor of Pharmacy degree in May 2022 from St. John's University College of Pharmacy and Health Sciences. As a risk management fellow, she takes part... Read More →

Pierre Engel

Senior Director Business Development, Centogene Gmbh, Germany

With over 15 years of sales and delivery experience in the field of epidemiology and real world evidence (RWE), I am a passionate leader in healthcare innovation and a trusted partner for global pharma accounts. As a Senior Principal Epidemiology at CENTOGENE, I am responsible for... Read More →

Emily Epstein

Clinical Behavioral Health Specialist, Weill Cornell Medicine, United States

Emily Epstein, LMSW, is a Clinical Behavioral Health Care Specialist at Weill Cornell Medicine's Genetics and Personalized Cancer Prevention Program (GPCP). The GPCP is committed to identifying individuals living at an increased lifetime risk for cancer, conducting research, and creating... Read More →

Samuel Ewusie

Associate Director, Safety Evidence and Science, Bristol-Myers Squibb Company, United States

A registered pharmacist with a PharmD and an MS in Global Clinical and Pharmacovigilance Regulations, experienced in Clinical Drug Safety and Pharmacovigilance, Risk Management including Risk Evaluation and Mitigation Strategy (REMS), Pharmacoepidemiology and Research Data analys... Read More →

Majdi Al Gharsan

Director, Director of Medical Services, Ministry of Defence, Saudi Arabia

Yogesh Gulati

Senior Safety Physician, Soterius, India

Cheryl Hergert

University of Southern California, United States

With over 25 years of experience working with small and large companies, Cheryl is familiar with product development for medical devices, pharmaceuticals, and combination products. Her experience ranges from product feasibility testing to product launch. She has held positions in... Read More →

Hisahiro Ito

Head of Project Management Office, National Cancer Center Japan, Japan

Frank Jaeger

Independent Consultant, Nanodose Therapeutics, United States

Frank Jaeger is an accomplished C-suite leader with over 25 years of biopharmaceutical tenure from seed-stage to large global pharma, in small and large molecules, and from pre-launch to in-market experience. His career spans across R&D, Medical Affairs, Business Development, Commercial... Read More →

Sung Hoon Jung

Professor, The Catholic University of Korea, Korea, Republic of

Sung-Goo Kang

Clinical Professor., St.Vincent's Hospital, The Catholic University of Korea, Korea, Republic of

Sarah Kang

Safety Evaluator, FDA, United States

Sarah Kang is a safety evaluator in the Division of Pharmacovigilance (DPV) within the Office of Surveillance and Epidemiology at the United States Food and Drug Administration in Silver Spring, Maryland. She has over 9 years of experience as a clinical pharmacist and over 8 years... Read More →

Joseph Laudano

Medical Director, IQVIA, United States

Joseph B. Laudano BS Pharm, Pharm D – Medical Director, IQVIA Inc. Joe has over 35 years’ experience in Pharma. Before joining IQVIA, he was VP, Medical Affairs at Pharmaspectra, VP Medical Affairs at Alliqua Biomedical and Senior Director of Medical Affairs & Global Head of Publication... Read More →

Christina Mack

Chief Scientific Officer, Real-World Solutions, IQVIA, United States

Christina Mack is Chief Scientific Officer of IQVIA real world solutions. An epidemiologist and engineer by training, she is responsible for driving scientific and technical innovation that directly impacts patient health. Recognized as a 2023 PharmaVoice100 Honoree, she’s committed... Read More →

Laura Magda

Director of Clinical Trials, SRI International, United States

Andrew Marley

Senior Epidemiologist, Parexel, Spain

Hotaka Maruyama

Division of PharmacoEpidemiology, Office of Pharmacovigilance ?, Pharmaceuticals and Medical Devices Agency (PMDA), Japan

I am a reviewer of pharmacoepidemiology division and have a few years' experience in the office of pharmacovigilance I at Pharmaceuticals and medical devices agency(PMDA).

Timothe Menard

Global Head, Quality Excellence Digital | Bioethics Coach (Data Ethics), F. Hoffmann-La Roche Ltd, Switzerland

Started in drug safety at Merck KGaA, joined Roche as a GCP/PV auditor. Transitioned to analytics; now heads Quality Excellence Digital. Focuses on digital & analytics for core quality deliverables. Co-founded the Inter coMPany quALity Analytics consortium to drive data/quality policy... Read More →

Mehdi Najafzadeh

Senior Director, Medidata AI, United States

Mehdi NajafZadeh, PhD, is Senior Director at Medidata AI. Before joining Medidata AI, he was an Assistant Professor of Medicine in the Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine, Brigham and Women’s Hospital and Harvard Medical School, and the... Read More →

Raphael Pareschi

Patient Safety Lead/ Head of Pharmacovigilance Brazil, Roche, Brazil

Raphael has more than 16 years of experience in Pharmacovigilance, beginning at Sanofi Brazil, where he acted in roles of increasing responsibility within local PV organization, responsibilities including oversight of case management, PSUR management and RMP management. Raphael also... Read More →

Izabela Pedro

Clinical Research Associate, Hospital Israelita Albert Einstein, Brazil

Gerd Rippin

Senior Director, Biostatistics, Real-World Solutions, IQVIA, Germany

Dr. Gerd Rippin is a trained statistician, receiving his statistics degree in 1995 from the University of Dortmund, Germany (equivalent to BSc and MSc), and his Dr. of Sciences (equivalent to PhD) in 1999 from the University of Mainz, Germany. Dr. Rippin has worked as a medical statistician... Read More →

Bruna Sampaio

Manager, Data management, Hospital Israelita Albert Einstein, Brazil

Bruna has over 14 years of professional experience with technology and data operations. Working in clinical research for almost 10 years, she is experienced in EDC Systems (first as a system analyst and later as an end-user), data management, and data analytics. Currently, she is... Read More →

Chris Schneiderman

Epidemiologist, Abbvie, United States

Samantha Seepersad-Nayee

AD, Excision Biotherapeutics, United States

Alexandru Socolov

Senior Data Scientist, Medidata Solutions, United States

Alexandru is a Senior Data Scientist at Medidata AI focused on building advanced analytical solutions to make clinical trials safer, cheaper and faster. With the background in operations research, mathematical optimization and machine learning, Alexandru applies newest techniques... Read More →

Hiroya Taniguchi

Department of Clinical Oncology, Aichi Cancer Center Hospital, Japan

Brittin Wagner

Senior Research Scientist, PointClickCare, Canada

Brittin Wagner is Senior Research Scientist at PointClickCare. She holds a PhD is in Sociology, PhD Minor in Social Statistics from the University of Washington, with postdoctoral training in health services research & development. She has a longstanding commitment to measurement... Read More →

Matt Wampole

Director, Solution Consulting, Clarivate, United States

Matt Wampole is the Director of Solution Consulting at Clarivate where he and his team supports clients from discovery to launch of new medical interventions. His 20 years of experience covered a broad range of topics across drug discovery and optimization, clinical trial optimization... Read More →

Susan Watson

Associate Director, Bioethics, Eli Lilly and Company, United States

Susan Briggs Watson, Ph.D. is an Associate Director of Bioethics at Eli Lilly and Company. She received a PhD in clinical psychology from Indiana University-Purdue University at Indianapolis (IUPUI) and completed Georgetown University's Intensive Bioethics Course 38. She has worked... Read More →

Sam Willcox

Section Manager - Large Molecule Bioanalysis, ACM Global Laboratories, United Kingdom

Sam graduated from the University of Hull with a BSc in Human Biology in 2009. Since graduating he has worked for the last 15 years in regulated bioanalysis supporting the drug development industry. Expert in the field of bioanalysis of large molecules via ligand binding assays he... Read More →

Rebecca Williams

Senior Clinical Trials Subject Matter Expert, Essex, Part of Emmes Group, United States

Rebecca Williams, PharmD, MPH, is a Clinical Trials Subject Matter Expert with Essex, Part of Emmes Group. In this role she supports strategic policy and data initiatives with the National Cancer Institute’s Coordinating Center for Clinical Trials. Prior to this role she was the... Read More →

18: Posters, Session

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