DIA 2018 Global Annual Meeting

Jasmine Benger is the Research Services Senior Project Manager at CISCRP. She is responsible for supporting the design, implementation, analysis and reporting of a variety of CISCRP research studies including the Perceptions & Insights studies and numerous Patient Advisory Boards... 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 →

Xiangchen (Bob) Cui, Senior Director, Head of Statistical Programming Department of Alkermes, Inc., has 19-year experience with 10+ years in managing various levels of programmers.He has very strong hands-on SAS skills for clinical trial reporting and tool development, and track record... Read More →

Aaron creates and deploys innovative and successful strategies that generate awareness and engagement surrounding clinical research for biopharm sponsors, advocacy organizations and patient thought-leaders. In 2018, Aaron launched BBK’s Pharma15 Live! web series -- a dynamic new... Read More →

Ellyn Getz is the Associate Director of Development and Community Engagement at CISCRP. She is responsible for directing CISCRP’s educational and outreach initiatives, including AWARE for All: Clinical Research Education Days, MT Pharmacy and Journey to Better Health mobile experiential... Read More →

Erik Hansen is a Clinical Study Manager at PRA Health Sciences in Salt Lake City, Utah. He has worked at PRA for 8 years, beginning in Quality Assurance and continuing as Project Supervisor before progressing to his current managerial position. He has co-authored several publications... Read More →

I'm working at Asan Medical Center as a Project Manager of Clinical trials.

Dr. Brad Jordan is a Director of Global Regulatory and R&D Policy at Amgen where his role focuses on global technical regulatory policy relating to biologics and biosimilars. Dr. Jordan joined Amgen in 2006, and prior to his role in Policy, spent 10 years in the Discovery Research... Read More →

Tanveer Khan is registered pharmacist, he has completed his Masters in Pharmacy with Pharmacology as specialization from NMIMS Mumbai. He has more than 10 years of experience in the field of Drug Safety and Pharmacovigilance. He holds a position of Manager, Pharmacovigilance at IQVIA... Read More →

Sanjeev is an MD in Internal Medicine and has more than 16 years’ experience in the field of Medicine, Pharmacovigilance and Clinical Research. He has held executive leadership positions in pharmaceutical companies and business process outsourcing firms with responsibilities for... Read More →

Cambrey Nguyen earned a Pharm.D. from the University of Kansas School of Pharmacy in 2012. After graduation, she worked for Walgreens then moved into the pharmaceutical industry as a Medical Information Specialist at ProPharma Group. At ProPharma Group, she managed clients that specialized... Read More →

Krystle Pianka is an experienced public health professional, having 14 years of experience in research and pharmaceutical industries with 10 years in global pharmacovigilance (GPV). She received her bachelor’s degree from the University of Pennsylvania in Biological Basis of Behavior... Read More →

Monika Schneider is a Managing Associate within the biomedical innovation team at the Duke-Margolis Center for Health Policy. Her work focuses incentive mechanisms and payment reform models that could encourage development in areas of medical unmet need. Monika's portfolio includes... Read More →

Meredith Smith is Global Risk Management Officer at Amgen, Inc. where she leads a team of 6 scientists responsible for medicinal product benefit-risk assessment and risk management. She is a behavioral scientist and health services researcher by training with over 15 years of experience... Read More →