Global Regulatory Affairs Post-Doctoral Fellow, Rutgers, The State University of New Jersey
Basirat Adeyemi is a pharmacist completing a Global Regulatory Affairs (GRA) post-doctoral fellowship at Merck & Co. Inc. partnered with the Rutgers Pharmaceutical Industry Fellowship (RPIF). She earned a Doctor of Pharmacy degree from Touro College of Pharmacy and a B.S. in Biology... Read More →
Catherine de Castro is a member of QuintilesIMS' Project Management Center of Excellence, which focuses on the continuous evolution of QI Project Leaders. Her expertise is in process improvement and strategic initiatives. In her current role she focuses on embedding project management... Read More →
Postdoctoral Fellow, Office of New Drugs, Center for Drug Evaluation and Research, FDA
I received my Ph.D. from the University of Toronto. During my graduate school training, I gained in-depth experience in designing and conducting clinical trials to investigate the efficacy and safety of a wide range of dietary supplements. I am currently a postdoctoral fellow at... Read More →
Post-PharmD Regulatory Affairs Fellow, Biogen; MCPHS University
Tina Chhabra is a Post-Doctoral fellow in Regulatory Affairs and Safety & Benefit-Risk Management with the Biogen-MCPHS University post-graduate fellowship program. She received her Bachelor's in Political Science and PharmD from Virginia Commonwealth University.
Deborah Covington, DrPH, is a senior research scientist at Evidera and part-time faculty at the University of North Carolina, Wilmington. She received her doctorate from the University of North Carolina, Chapel Hill and has 30+ years of epidemiological research experience focusing... Read More →
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 →
Meghan Donahue is the Solution Design Studio Manager at QuintilesIMS. In this role, she leads collaborative workshops utilizing user-centric methodologies, markets the Design Studio's capabilities, actively networks to establish strategic relationships, and evaluates emerging technology... Read More →
Owner, Emerson Consulting & Clinical Research Services
Dr. Emerson is an Epidemiologist and Registered Nurse with 15 years' industry experience. She worked in Oncology Clinical Research as both a CRA and Project Manager before moving over to the Quality Management side of the business. Dr. Emerson is now the owner of ECCRS, an international... Read More →
Dr. Gewanter is a pediatric rheumatologist and current chair of ASBM. A graduate of Duke University and Wayne State University School of Medicine, he received his pediatric and rheumatology training at the University of Rochester/Strong Memorial Hospital. He has practiced in Richmond... Read More →
Senior Director, Standards Development & Education, CDISC
Kit Howard has over 30 years’ experience in many areas of research and development, including developing data and process standards for exploratory through post-marketing human clinical research, pharmacogenomics and non-clinical research. She is CDISC's Senior Education Expert... Read More →
Candice M Hughes, PhD, MBA, is a strategy and management consultant helping with Alliance Management for biopharma firms via Hughes BioPharma Advisers. She is also a serial entrepreneur who founded a digital health startup. She has worked with over a third of the top 25 global pharma... Read More →
Office of Medical Informatics and Epidemiology, Pharmaceuticals and Medical Devices Agency (PMDA)
Ms. Maori Ito is currently working as a safety evaluator at the Office of Medical Informatics and Epidemiology of Pharmaceuticals and Medical Devices Agency (PMDA). Having graduated from the master course of Computational Biology at Tokyo University, she joined the National Institute... Read More →
Regulatory Affairs Post-PharmD Fellow, Alnylam Pharmaceuticals, Inc.
Dayna graduated with her PharmD in May of 2016 and is currently completing a 2-year Fellowship in Regulatory Strategy at Alnylam Pharmaceuticals, a pre-commercial biotechnology company developing RNA interference (RNAi) in the rare disease space. Dayna's focus at Alnylam so far has... Read More →
Head, Regulatory Collaborations, Centre for Innovation in Regulatory Science (CIRS)
Dr Liberti has worked in pharmaceutical regulatory affairs, communications and clinical R&D for the past four decades. Since 2009 he has served as the Executive Director of CIRS (the Centre for Innovation in Regulatory Science, Ltd, forming part of Clarivate Analytics). He has been... Read More →
Jenny Ly is currently a Senior Clinical Science Advisor at ERT. She is a neuropsychologist with over 15 years of experience in the management and design of clinical trials. She has extensive experience consulting on best practices for eCOA design/implementation and developing training... Read More →
Post-Doctoral Fellow, Rutgers, The State University of New Jersey
I am a second year Medical Affairs post-doctoral fellow within the Rutgers Institute for Pharmaceutical Industry Fellowships in partnership with Pfizer Consumer Healthcare. I am a pharmacist by training and I am interested in Medical Affairs, Medical Information, and Outcomes Res... Read More →
Post-Doctoral Fellow, Rutgers, The State University of New Jersey
Daina Nanchanatt joined the Rutgers University Pharmaceutical Industry Fellowship Program in partnership with Bayer Consumer Health in 2016. She is currently completing a two year fellowship with the Innovation and Development Category Leadership team at Bayer. Daina earned her Pharm.D... Read More →
More then 18 years Clinical Trials experience, trained in family medicine, doctural degree in Pharmacology and Molecular Biology, NIH Fellowships in cancer and aging.
Srinivas is currently leading the initiatives focused on building site relationships and partnerships through a team of Alliance managers working closely with Quintiles preferred sites besides leading the CTE/NE offering in Asia Pac. He has 25 years of combined global biopharmaceutical... Read More →
Regulatory Affairs Postdoctoral Fellow, GlaxoSmithKline, University of North Carolina-GlaxoSmithKline
Masooma Razvi received her Doctor of Pharmacy degree from the University of Illinois at Chicago and completed a PGY1 general practice pharmacy residency at Wheaton Franciscan Healthcare in Milwaukee, Wisconsin. She is currently finishing up the second year of her Regulatory Affairs... Read More →
Health Scientist Administrator, NIAID, Clinical Research Resources Branch, National Institutes of Health (NIH)
Dr. Shah is a Regulatory Affairs professional with over 18 years of experience ranging from basic research through product development. Dr. Shah's experience as the Regulatory lead is varied and includes clinical trials for drugs and biologics in various therapeutic areas from diabetes... Read More →
Postdoctoral Fellow, Office of New Drugs, CDER, FDA
Jennifer Shing received her Ph.D. in Molecular Pharmacology and Experimental Therapeutics from Mayo Clinic Graduate School of Biomedical Sciences. She is currently an Oak Ridge for Science and Education Fellow at the U.S. Food and Drug Administration (FDA), where she performs scientific... Read More →
Scott earned his PharmD at Midwestern University’s Chicago College of Pharmacy. He has worked in pharmaceutical industry at AbbVie within Pharmacovigilance and Patient Safety, Global Medical Information, and Regulatory Affairs. Scott currently works as a Senior Safety Data Scientist... Read More →
Judith Thompson was born and raised in Atlanta, GA. She studied pharmacy at Xavier University of Louisiana College of Pharmacy and proceeded to work in a fast-paced environment, assuring positive patient impact in retail and clinical pharmacy settings. Passionate about patients, the... Read More →
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 →
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 →
Zhongwei has worked more than 23 years in different major pharmaceutical companies across both Rx and OTC fields, and has become a "world-class" SAS programmer in clinical trial.
Tuesday June 20, 2017 9:30am - 5:00pm CDT
Poster Area Exhibit HallMcCormick Place 2301 South Martin Luther King Jr. Drive, Gate 4 Chicago, IL 60616
