DIA 2017 Annual Meeting

?Kamal leads digital health projects in Roche's Research and Early Development Informatics (pREDi) organization. He is ??responsible for ?project management and execution of digital projects? by ??identifying new ?innovative ?technology? ???and developing services. His focus is on... Read More →

David Bristol has been a statistical consultant for more than 10 years, currently as Statistical Consulting Services. Prior to consulting, he was a statistician in the pharmaceutical industry for more than twenty years in several therapeutic areas at six different companies. He has... Read More →

Dr Magda Bujar is Senior Manager, Regulatory Programme and Strategic Partnerships and has over 8 years’ experience working in Regulatory Policy and Science. She has co-authored a number of publications and has presented and chaired at major scientific meetings including those of... Read More →

I am leading the global team here at SOUSEIKAI.My background is in neuropharmacology, but now I feel privileged witnessing and being part of the process of developing new and innovative treatments against human diseases in all therapeutic areas.It would be great to learn more about... Read More →

Kevin Craig is a senior medical director in Early Clinical Medical and Scientific Services at Covance. Prior to 2017, he worked in the late-stage neuroscience group. Prior to joining Covance in 2011, Dr Craig worked with a pharmaceutical consortium to develop and commercialize translational... Read More →

Nancy Dreyer is the Global Chief of Scientific Affairs for QuintilesIMS Real-World Insights, and heads the Center for Advanced Evidence Generation. She leads an international team conducting research on the safety, effectiveness, and value of medical treatments using secondary and/or... Read More →

I am a Global Regulatory Affairs Fellow at the University of North Carolina. Through this program, I receive academic regulatory experience at UNC's clinical research facilities as well as industry training through GlaxoSmithKline. I specialize in respiratory and immuno-inflammation... Read More →

"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 →

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 →

Khairul is the Head of Business Development in Clinical Research Malaysia, a non profit company which is set up by Ministry of Health Malaysia to spearhead the national agenda for clinical research. He leads a team which drives the business as well as providing complementary feasibility... 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 →

Anastasia is currently a Post-Doctoral Fellow in Medical Affairs with the Alnylam Pharmaceuticals and Northeastern University Fellowship Program in Cambridge, MA. As part of her program, Anastasia plays an active role within the Medical Affairs team as well as teaching and facilitating... Read More →

Andrew Melli is the Senior Manager of Global Clinical Development at SOUSEIKAI Global Clinical Research Center, serving as both liaison for international business development and investment, as well as an active member of the clinical trial team. It is his hope to help bridge the... Read More →

As a former study coordinator for 3 different SOUSEIKAI clinical research units (Kyushu Pharmacology Research Clinic, Sugioka Memorial Hospital, PS Clinic), this experience has grounded his overall view and understanding of the clinical trial process from early phase to post-marketing... Read More →

Saumya has >10 yrs. of clinical research experience including tenures at QuintilesIMS & Parexel. In her current role, she is leading the operations team responsible for optimal delivery of recruitment campaigns. She has hands-on experience developing best-in-class recruitment strategy... Read More →

I obtained my PharmD from the Purdue University College of Pharmacy and now pursuing a fellowship in Clinical Sciences and Innovation with Novartis Institutes for Biomedical Research (NIBR) and the Massachusetts College of Pharmacy and Health Sciences (MCPHS).

Dawn Niccum is the associate director of quality at Endocyte, where she is responsible for GCP compliance, SOP development, computer system validation oversight, and training. With over 20 years of pharmaceutical experience, Ms. Niccum holds a Master’s Degree in Regulatory Affairs... Read More →

Dawn Niccum is Director, Quality Assurance for the inSeption Group and responsible for all areas of QA including compliance, Policies and SOPs, and training. She was formerly with Endocyte, Inc. With over 20 years of pharmaceutical experience, Ms. Niccum holds a Master’s Degree... Read More →

Dr. Darin Oppenheimer is an Executive Director of the Drug Device Center of Excellence focusing on Medical Devices and Combination products at Merck. After spending 15 years working in Regulatory Affairs and Development for various organizations within the Medical Device and Pharmaceutical... Read More →

Shivam Kamlesh Patel earned his doctorate in pharmacy from the Ernest Mario School of Pharmacy at Rutgers University in 2016. He is currently completing his fellowship in global regulatory affairs with the University of North Carolina at Chapel Hill. His experiences in the fellowship... Read More →

Kiyoteru Takenouchi, Ph.D. is CDISC Program Coordinator, Division of Global Affairs in Translational Research Informatics Center (TRI) in Japan. Dr. Takenouchi was former CDISC Board of Directors for 6 years. He has over 25 years of experience in the area of clinical research, including... Read More →

25 years of experience in Contract Research Organization (CRO) environment working with clinical trials globally for pharmaceutical, biotech, generic, and consumer product industries in study design, treatment randomization, data analysis and report writing. Lead projects in the execution... Read More →

Founder and president of Whitsell Innovations, Inc., a medical writing firm headquartered in Chapel Hill, NC, Ms. Whitsell has over 25 years of experience, specializing in global submission strategy, regulatory medical writing, emerging technologies, and data visualization. Prior... Read More →

John Willmore is co-founder of BizInt Solutions Inc., and manages the development of all aspects of the BizInt Smart Charts product line. John has a B.S. in Electrical Engineering from Rice University and over 25 years experience in software development. Outside of work, John plays... Read More →

Dr. Robert Wittenberg works in regulatory affairs in Labeling, Advertising, and Promotion for new drugs and devices. He is an adjunct clinical instructor at the University of Illinois at Chicago, College of Pharmacy (UIC COP), where he earned his PharmD. Upon graduating from the UIC... 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 →