Venky Chakravarthy

About Venky Chakravarthy

As an Associate Director of Statistical Programming at Takeda, I lead a team of SAS programmers who support the analysis and reporting of clinical trial data for oncology studies. I have over 20 years of experience in statistical programming, data analysis, and validation for various phases and therapeutic areas of clinical research.I am passionate about delivering high-quality and timely results that meet the regulatory and scientific standards and expectations of our clients and stakeholders. I leverage my expertise in SAS, CDISC, and statistical methods to create and review datasets, tables, figures, and listings for efficacy and safety outcomes. I also provide vendor oversight and submission activities to FDA, EMA, and other agencies. Additionally, I am a seasoned remote worker who collaborates effectively with global and cross-functional teams. I have presented and published multiple papers on various topics related to SAS and statistical programming at industry conferences and forums.

Experience

1. Associate Director, Statistical Programming

   Takeda

   Jul 2020 — Present

Education

• Loyola College

  M.A., Social Work

• Ramakrishna Mission Vivekananda College

  B.A., Economics

• Jack, Joseph and Morton Mandel School of Applied Social Sciences at CWRU

  Ph.D, Social Welfare

Skills

• Data Management
• 21 Cfr Part 11
• Infectious Diseases
• Clinical Trials
• Statistical Programming
• Sas
• Oncology
• Regulatory Submissions
• Data Mining
• Validation
• Clinical Data Management
• Statistical Modeling
• Medical Writing
• Biostatistics
• Edc
• Ctms
• Clinical Research
• Drug Development
• Clinical Development
• Gcp
• Sas Programming
• Pharmaceutical Industry
• Sop
• Fda
• Regulatory Affairs
• Lifesciences
• Data Analysis
• Life Sciences
• CRO
• Analytics
• Biotechnology