Richard Wu
Consultant@ Celgene
Richmond, Virginia, United States
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Richard Wu is a highly experienced professional with 14.7 years of work experience in the pharmaceutical industry. He has a strong background in clinical studies, with expertise in areas such as Efficacy and Safety analysis, FDA submissions, and SAS Macros development. Richard has worked as a consultant at Celgene, Chiltern, inVentiv Health, and Amgen, where he has contributed to various clinical studies and FDA submissions. He is also a certified SAS professional and has a deep understanding of the therapeutic area of Oncology, CNS, Infections, Vaccine, Cardiovascular, and Genetics.
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Emails and Phone Numbers

@celgene.com
+1 908673****
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About

* 17 years pharmaceutical industry experience in clinical studies (Phase I, II, III and IV, ISS/ISE, NDA, Efficacy and Safety analysis) * Served as lead programmer for multiple clinical studies and ISS * Expert in CDISC (SDTM/ADaM) * Was in charge of 40+ studies SDTM and ADaM FDA submissions * Extensive experience in SAS Macros development * Extensive experience in statistical analyses * Managed CRO outsourcing studies with quality controlling and timeline planning * 19 years of experience in SAS programming (V9.2/9.3/9.4) * SAS Certified Professional, 1999 (SCP Certificate) * Therapeutic area: Oncology, CNS, Infections, Vaccine, Cardiovascular, Genetic, etc.

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Work Experience

86 Morris Avenue, Summit, New Jersey, 07901, US

Pharmaceutical Manufacturing

2667
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Richard Wu's Professional Milestones

  • Consultant (2019-01-01~): Provided expert guidance to clients, ensuring their needs are met and driving successful completion.
  • Principal Statistical Programmer (2017-04-01~): Developing and implementing scalable and efficient analysis frameworks to enhance data processing efficiency and decision-making capabilities.
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