Alberto Grignolo,
PhD
Corporate Vice President
PAREXEL International
Dr. Alberto Grignolo is currently a Corporate Vice President at PAREXEL International, where he has worked for the past 25 years, and most recently established the firm’s Japan Consulting Services during a two-year assignment in Tokyo. He participates actively in PAREXEL’s Diversity and Inclusion initiatives and in corporate efforts to promote and maintain a High Performance Culture and excellent customer service.
He was previously President of FIDIA Pharmaceutical Corporation and held positions in regulatory affairs at Smith Kline & French Laboratories. He has served as an adviser to the Institute of Medicine of the National Academy of Sciences on human subject protection in clinical trials, and is a former member of the first Executive Committee of the Clinical Trials Transformation Initiative (CTTI). Dr. Grignolo has served as a leader of several industry organizations, including as Chair of the DIA Board of Directors, and Chairman of the Regulatory Affairs Professionals Society.
A member and volunteer with DIA for over 30 years, Dr. Grignolo serves on the faculty for DIA’s Regulatory Affairs: The IND, NDA, and Postmarketing training course and has taught this course numerous times in Japan, China, Korea, Europe and the United States for more than a decade. Dr. Grignolo has been a frequent Speaker, Program Chair, Session Chair or Instructor at international conferences, seminars, workshops and courses on Drug Development and Regulatory Affairs. He was Program Chair of the DIA 2007 Annual Meeting and is currently the Editor of Global Forum, DIA’s digital magazine. He received DIA’s Global Inspire Award (Global Connector) in 2015.
Dr. Grignolo earned his BS degree from Duke University and his PhD in Psychology from the University of North Carolina at Chapel Hill. He completed postdoctoral work in neuropharmacology at Duke University Medical Center.
Fellows of DIA
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Tatsuo Kurokawa,
PhD •Chair, Fellows of DIA
President, Japan Self-Medication Industry -
Martin Harvey Allchurch • Principal International Affairs Officer, European Medicines Agency, European Union
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Minnie Baylor-Henry,
JD • President, B-Henry & Associates -
Gaby Danan,
MD, PhD • Pharmacovigilance Expert -
Richard Day,
MD • Professor of Clinical Pharmacology, St. Vincent's Hospital -
Marie Dray,
MBA • President, International Regulatory Affairs Group LLC -
Nancy A. Dreyer,
MPH, PhD • Global Chief, Sci Affairs; Sr VP, Head, Center for Advanced Evidence Generation
IQVIA -
Ron Fitzmartin,
PhD • Senior Advisor, Strategic Programs,Center for Drug Evaluation and Research, US Food and Drug Administration -
E. Stewart Geary,
MD • Senior VP, Chief Medical Officer, Director, Corporate Medical Affairs HQ, Eisai Co., Ltd. -
Ken Getz,
MBA • Chairman, CISCRP; Director of Sponsored Research, Tufts Center For the Study of Drug Development -
Alberto Grignolo,
PhD • Corporate Vice President
PAREXEL International -
Yves Juillet,
MD • Senior Vice-President, Industrie Sante -
Sandra L. Kweder,
MD • Deputy Director, FDA Liaison to the EMA, Office of International Programs, OC -
Murray M. Lumpkin,
MD • Deputy Director, Integrated Delivery, and Lead for Global Regulatory Systems Initiatives
Bill and Melinda Gates Foundation -
Sandra A. Milligan,
MD, JD • Senior Vice President, Head of Global Regulatory Affairs and Clinical Safety, Merck & Co., Inc. -
Noriaki Murao,
MS • Representative, NM Consulting -
Jennifer Riggins,
PhD • Advisor, Digital Channels and eCapabilities, Eli Lilly and Company -
Jeffrey Sherman,
MD • Chief Medical Officer & EVP, Horizon Pharma, Inc. -
Per Spindler,
DVM, MBA • Director Biopeople, University of Copenhagen -
Ling Su,
PhD • Professor and Director, Institute of Drug Regulatory Science, Shenyang Pharmaceutical University, Venture Partner, Lilly Asia Ventures