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Wednesday, June 26 • 9:00am - 4:00pm
Professional Poster Session 2

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Component Type: Poster Presentation




Speakers
avatar for Chelsea Aiudi

Chelsea Aiudi

Associate Director, Medical Information, Array BioPharma
avatar for Sharon Hensley Alford

Sharon Hensley Alford

Offering Management, IBM Watson Health
Sharon Hensley Alford, PhD is Associated Chief Health Officer for Data & Evidence within the Life Science (LS) pillar of IBM Watson Health. Dr. Alford has been working on data and analytic strategy for life science clients since she joined IBM 2+ years ago. Prior to IBM, she worked... Read More →
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Hamad Alyami

Assistant Professor, Najran University
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Lauren Aronin

Postdoctoral Fellow, St. John's University
avatar for Linda Brennan

Linda Brennan

Director, Community Partnerships, Cystic Fibrosis Foundation
Linda Brennan is Senior Director, Community Partnerships at the Cystic Fibrosis Foundation (CFF), which brings the perspectives of people affected by cystic fibrosis (CF) into all the Foundation’s activities, including research and clinical development, and provides opportunities... Read More →
avatar for Magda Bujar

Magda Bujar

Manager, Strategic Development, Centre For Innovation In Regulatory Science (CIRS)
Dr Magda Bujar is a Manager, Strategic Development at CIRS. In her current role, she is responsible for developing and executing strategies for engaging with CIRS stakeholders - pharmaceutical companies as well as major regulatory authorities. Magda also initiates and coordinates... Read More →
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Lois Castellano

Senior Specialist, Global CMC Regulatory Affairs, Merck & Co., Inc.
Lois Castellano is currently a Senior Scientist in Global Regulatory Affairs with Merck & Co. She is a chemical engineer by discipline, and holds a B.S. in Chemical Engineering from Cornell University and a Masters in Business and Science from Rutgers University. Lois has a broad... Read More →
avatar for Jennifer Cichone

Jennifer Cichone

Otsuka Pharmaceutical Development and Commercialization Inc.
Jennifer Cichone joined Otsuka Development & Commercialization (OPDC) as Director in Global Pharmacovigilance in 2013. She has experience in Pharmacovigilance for the past 16 years, specifically in the aggregate reporting and risk management plans space. In addition, Jennifer is a... Read More →
avatar for Nadeeka Dias

Nadeeka Dias

Sr. Scientific Advisor, ERT
Nadeeka Dias is a clinical neuroscientist with 8 years of in-depth experience in the design and management of human clinical research. She has extensive expertise in psychiatry and neuropharmacology, as well as proficiency with clinical outcome assessments and rater training in a... Read More →
AD

Alexandra Didonato

Post-doctoral Fellow, St. John's University
Alexandra DiDonato, Pharm.D., is the 2018-2020 St. John's University/Allergan fellow in Regulatory Affairs - Advertising and Labeling. She received her Doctor of Pharmacy Degree from St. John's University College of Pharmacy and Health Sciences. During her time at St. John's, Alexandra... Read More →
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Kelly Dumais

Clinical Science Advisor, ERT
avatar for Matthew Eberle

Matthew Eberle

Lead Developer, Analytics & Custom Solutions, BizInt Solutions, Inc.
"Matt Eberle is an information professional with over ten years spent in the pharmaceutical industry, where he held positions of Senior Information Scientist and Pharmaceutical Information Analyst. He has worked with groups across the organization, from early R&D to legal and clinical... Read More →
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Hui-Chun Hong

Pharmacokinetic Reviewer, TFDA/Center for Drug Evaluation
Hui-Chun Hong is currently a Pharmacokinetic Reviewer at Center for Drug Evaluation, Taiwan. Her work focuses specifically on review of New Drug Application (NDA), Clinical Trial Protocol of Investigational New Drug (IND) and Bridging Study Evaluation (BSE). Hui-Chun holds a MS in... Read More →
VJ

Vivien Jagalski

Regulatory Intelligence Professional, Lundbeck
I have graduated with a PhD in biophysics and joined Lundbeck in 2017. From the start I support regulatory strategy decisions, clinical development and projects with data tools and analysis to help making informed decisions and reflect regulators current thinking on a range of topics... Read More →
FJ

Fred Jerva

Pharmacovigilance, AstraZeneca
Dr. Fred Jerva is a pharmacovigilance scientist at AstraZeneca and holds a PhD in Pharmacology from Yale and a PharmD from Creighton. He is an experienced pharmaceutical professional having worked across R&D at Pfizer, GlaxoSmithKline and AstraZeneca. Originally trained in pharmacology... Read More →
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Min Kyung (Amy) Kim

Post-Doctoral Fellow, Rutgers University/Ernest Mario School of Pharmacy
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Bhavish Lekh

Feasibility Manager, Synteract
Bhavish Lekh has over 5 years of experience working in clinical research, health care and biochemistry. In his current role, he provides expert feasibility guidance to clinical research studies and programs, to develop the most effective country and site strategies. Bhavish has experience... Read More →
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Nicole Li

Principal Scientist, Merck & Co., Inc.
GL

Gaoyang Li

Lead SPA, Bayer
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Wen Liu

Principal Scientist, Merck & Co., Inc.
CM

Christine Maccracken

Director, Patient Support, Janssen
AM

Austin Marrazza

Student, Pennsylvania State University
My name is Austin Marrazza and I am from Whitehouse Station, New Jersey. I am currently a rising senior at Penn State University majoring in Neuroscience. After college, I have plans to pursue a PhD in Neuroscience as well.
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Marie McCarthy

Senior Director of Product Innovation, ICON plc
Marie Mc Carthy, Senior Director of Product Innovation, is part of the multidisciplinary Innovation Team at ICON PLC. Her previous role was that of EU Sales and Marketing Manager with Philips Respironics, building awareness of the value of Actigraphy endpoints among Clinicians and... Read More →
AM

Alexis Miller

Senior Director, Regulatory Science and Policy, Sanofi
Alexis is a Senior Director for Sanofi Global Regulatory Science & Policy, helping to shape the regulatory and policy environment on topics like patient-focused drug development, digital health technology regulation, and various PDUFA initiatives and FDA program implementation. Prior... Read More →
RM

Ruta Mockute

PV Innovation Senior Specialist, Celgene Corporation
I am a Sr. Specialist in Celgene's Global Drug Safety & Risk Management Innovation group leading a research and publications workstream that aims to disseminate data and evidence about our research in innovation, automation, machine learning, change management, and artificial intelligence... Read More →
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Colin Neate

Biostatistics Associate Director, Roche
Colin has worked as a Biostatistician in the Pharmaceutical Industry for more than 15 years. He is currently an Associate Director leading a team of Biostatisticians in oncology drug development in Roche's growing Product Development group in Mississauga, Canada. Prior to this, Colin... Read More →
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Kun Nie

Clindata Insight Inc
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Stephan Palm

Analyst, Clinical Sciences, Trinetx
AP

Alyssa Peechatka

Clinical Science Advisor, ERT
VQ

Victoria Quang

Post-Doctoral Fellow, Rutgers University/Ernest Mario School of Pharmacy
HR

Heather Romero

Clinical Scientist eCOA, WCG Medavante-Prophase
Heather Romero, PhD is an electronic clinical outcome assessment (eCOA) Clinical Scientist and neuropsychologist at MedAvante-ProPhase, a WIRB-Copernicus Group company. I provide scientific expertise for CNS clinical trials and collaborate with other industry leaders to shape COA... Read More →
MS

Michael Sadler

Clinical Science Advisor, ERT
Dr. Michael Sadler is a clinical research psychologist and an experienced consultant to global pharmaceutical industry in clinical trial outcomes measurement, clinician-rated assessments and patient-reported outcomes across therapeutic areas; health-related quality of life measures... Read More →
avatar for Michael Severo

Michael Severo

Post-Doctoral Fellow, Medical Affairs, Novartis Oncology/Rutgers University
Michael Severo is a Post-doctoral Fellow at Novartis Oncology in US Scientific Communications through the Rutgers Pharmaceutical Industry Fellowship Program. He received his Bachelor of Science (B.S.) degree in Pharmaceutical and Healthcare Studies, as well as, his Doctorate of Pharmacy... Read More →
CS

Caitlin Skenyon

Regulatory Affairs Fellow, Northeastern University
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Sally Stansbury

Medical Information Lead, Takeda
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Stephen Sun

Chief Medical Officer, Quality Risk Management Group, InVentiv Health Clinical
avatar for Thaddeus Urban

Thaddeus Urban

Sr. Clinical Data Manager, Syneos Health
Thaddeus Urban joined inVentiv Health (now Syneos Health) in 2016 and has worked two years assessing risk in phase II-III trials and for regulatory purposes. Prior to Syenos Health, he spent four years of working as a Clinical Data Coordinator across phases II-III, and two years of... Read More →
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Julienne Vaillancourt

Rare Disease Liaison, CBER, FDA
As the Rare Disease Liaison for FDA’s Center for Biologics Evaluation and Research (CBER) in the Office of the Director, CAPT Julienne Vaillancourt coordinates CBER's Rare Disease Program, which facilitates the development and timely approval of biologics for adults and children... Read More →
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Ria Westergaard

Clinical Pharmacist, Express Scripts
Ria Westergaard is the clinical lead for Express Scripts Data & Analytic Solutions team. By consulting with clients, Ria offers innovative ideas for gleaning insights from pharmacy claims data and improving project performance. She ensures clinical accuracy while developing creative... Read More →
avatar for Rinah Yamamoto

Rinah Yamamoto

Senior Clinical Scientific Advisor, ERT
Dr. Yamamoto holds a PhD in Experimental Psychology from Tufts University. She has experience in pre-clinical and clinical research in mood and anxiety disorders, substance use disorders, incentive salience, interactions of nutrition and behavior, and functional and pharmacological... Read More →
avatar for Mary Nilsson

Mary Nilsson

Statistician, Eli Lilly and Company
Mary received a MS degree in statistics from Iowa State University in 1989. She has been employed at Lilly since 1989 and is currently a research advisor in the Safety Analytics group within the Statistical Sciences function. She consults with compound teams on safety analysis planning... Read More →
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Stephen Sun

Vice President, Quality Risk Management, Syneos Health
Dr. Sun earned his Bachelors of Science in Chemistry, Food, and Nutrition from Rutgers University, his medical degree from Rutgers-New Jersey Medical School, and his Masters in Public Health from the Johns Hopkins Bloomberg School of Public Health. He has led various teams in pharmaceutical... Read More →
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Thomas Wasser

Senior Principle Scientist, Biostatistics, Consult-Stat: Complete Statistical Services
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David Lacagnina

President, The Eclinical Agency


Wednesday June 26, 2019 9:00am - 4:00pm
Posters Exhibit Hall San Diego Convention Center 111 W Harbor Drive, San Diego, CA 92101 USA