Senior Clinical Data Strategist

7 days ago


Hyderabad, Telangana, India Bristol Myers Squibb Full time
Transforming Patients' Lives through Science

Bristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. Our team of passionate and innovative professionals works tirelessly to develop cutting-edge treatments that make a real difference in people's lives.

Job Summary

We are seeking an experienced Senior Clinical Data Strategist to join our Global Biometrics & Data Sciences team. As a key member of our team, you will be responsible for providing functional expertise and leadership to clinical project teams, driving the design, development, and implementation of technical solutions for integrating, analyzing, and reporting clinical data.

The ideal candidate will have at least 10 years of programming experience in industry, including support of significant regulatory filings, and a proven track record of managing technical professionals in a regulated environment. You will be proficient in SAS and other software tools, with a broad expertise in statistical programming and computing strategies. Your ability to work effectively within cross-functional teams, communicate complex ideas simply, and drive process improvements will be invaluable to our organization.

Responsibilities
  • Provides comprehensive programming leadership and support to complex clinical project teams and vendors.
  • Drives the development and implementation of innovative strategies and technologies for clinical trial programming.
  • Independently develops, validates, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and standards.
  • Liaises with internal stakeholders, including Therapeutic Area Heads and Statistical Programming leadership, to ensure alignment and coordination across teams.
Requirements
  • Bachelor's degree in statistics, biostatistics, mathematics, computer science, or life sciences required.
  • At least 10 years of programming experience in industry, including support of significant regulatory filings, and a proven track record of managing technical professionals in a regulated environment.
  • 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.
  • Broad expertise in statistical programming and computing strategies.
Benefits
  • A competitive salary range of $140,000 - $170,000 per annum, depending on experience.
  • A comprehensive benefits package, including health insurance, retirement savings plan, and paid time off.
  • The opportunity to work with a talented and diverse team of professionals who share your passion for innovation and excellence.


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