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This workshop will be conducted in Japanese Language only.
Who should attend?
• Clinical research associate, site monitor
• Study manager, study leader
• Clinical development professional
• Clinical research coordinator
• Clinical data manager
• Clinical development related IT professional
• QC/QA professional
• Regulatory affairs professional
Keiichi Inaizumi, MSc • Japan Clinical Project Manager, Clinical Operations and Compliance 1
Pfizer R&D Japan, Japan
Yukihiro Matsuda, MSc • Project Manager, Project Leadership
PRA Health Sciences K.K., Japan
Toshiya Hara • Executive Vice President
I'rom Co., Ltd., Japan
Mitsuo Hayashi, MSc, RPh • Director & Head, Clinical Enablement
MSD K.K., Japan
Toshiko Ishibashi, PhD, RN • Associate Director,Oncology Medical Science Department
Daiichi Sankyo Co., Ltd., Japan
Aki Kitabayashi • Inspector, Office of Non-clinical and Clinical Compliance
Pharmaceuticals and Medical Devices Agency (PMDA), Japan
Akiko Kitagawa • Corporate Officer, Deputy Head, Business Operation Headquarters
EPS International Holdings Co., Ltd., Japan
Nobuhiro Koga, MBA, PMP • Director, International Center for Therapeutic Research - Japan
Nihon Servier Co., Ltd., Japan
Noriko Morishita, MSN • Manager, Clinical Trial Promotion Office
National Hospital Organization Headquarters, Japan
Satoshi Saeki, MSc • Executive Director, Head of Japn Operational Excellence, Medical Affairs, Japan
Astellas Pharma Inc., Japan
Norio Shimazaki • Director, Regional Clinical Operations Japan, Korea and Taiwan
Bristol-Myers Squibb K.K., Japan
Tsuyoshi Teramoto, PhD •
Toyama University Hospital, Japan
Miyoko Yamauchi • Group Manager, Clinical Research Dept.1
Chugai Clinical Research Center Co., Ltd. , Japan
Eri Sekine • Region Head, Trial Monitoring, Japan Development, Global Development Ops.
Novartis Pharma K.K., Japan