Program Manager for Data Science and Statistical Analysis

5 days ago


Hyderabad, Telangana, India Bristol Myers Squibb Full time

Bristol Myers Squibb is a leading global biopharmaceutical company with a strong commitment to innovation and excellence. As a Senior Manager, Statistical Programming, you will play a critical role in driving the development of cutting-edge statistical programming solutions that support the approval and market acceptance of our products.

About the Role

This is an exciting opportunity to join our team of experts in data science and statistical analysis. You will be responsible for providing comprehensive programming expertise to clinical project teams, leading statistical programming teams, and supporting the development, regulatory approval, and market acceptance of Bristol Myers Squibb products. Your primary focus will be on designing, developing, and implementing technical solutions for integrating, analyzing, and reporting clinical data.

Key Responsibilities
  • Provide leadership and support: Deploy programming strategies, standards, specifications, and programmed analysis to comply with regulatory requirements, SOPs, and work practices.
  • Develop complex programs: Independently develop, validate, troubleshoot, and maintain complex programs and utilities in accordance with predefined specifications and standards.
  • Electronic submission preparation: Lead or support the electronic submission preparation and review process.
  • Programming specifications: Develop unambiguous and robust programming specifications (e.g., ADaM specifications).
  • Review key planning documents: Review key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to align with project objectives and ensure clarity and completeness of programming assumptions and requirements.
Requirements
  • Bachelor's degree: Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences.
  • Programming experience: At least 9+ years of programming experience in industry, including support of significant regulatory filings.
  • Industry knowledge: Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical concepts, and medical terminology used in the analysis and submission of clinical data.
  • SAS proficiency: Demonstrated proficiency in using SAS to produce analysis datasets and TFLs, as well as other software tools and applications (e.g., MS office, XML, Pinnacle 21).
Preferred Requirements
  • Management experience: Management experience supervising technical professionals.
Compensation

The estimated salary for this position is $180,000 - $220,000 per year, depending on experience and qualifications.



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