Associate Director Statistical Programming

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Associate Director, Statistical Programming

As an Associate Director, Statistical Programming, you'll provide functional expertise and leadership to clinical project teams. You'll support the development, regulatory approval, and market acceptance of Bristol Myers Squibb products, designing and implementing technical solutions for clinical data integration, analysis, and reporting. You'll foster innovation in clinical trial programming and collaborate within Global Biometrics & Data Sciences (GBDS) and beyond.

Key Responsibilities

Project Responsibilities:

  • Lead comprehensive programming efforts for complex clinical projects, ensuring compliance with regulatory standards and internal processes.
  • Drive innovative programming strategies and technologies for clinical trials.
  • Develop, validate, troubleshoot, and maintain complex programs and utilities.
  • Oversee electronic submission preparation and review.
  • Create detailed and precise programming specifications.
  • Review and align planning documents with project goals, ensuring clarity and completeness.

Improvement Responsibilities:

  • Identify and lead process and technology enhancement initiatives.
  • Communicate proactively to address issues and support remediation efforts.

Managerial Responsibilities:

  • Recruit, manage, develop, and retain team members, enhancing their skills and capabilities.
  • Conduct performance reviews, set objectives, and offer real-time coaching and feedback.
  • Align team performance with company policies and objectives.
  • Maintain strong communication with stakeholders to ensure alignment of cross-functional strategies.

Minimum Requirements

  • Bachelor’s degree in statistics, biostatistics, mathematics, computer science, or life sciences.
  • 10+ years of programming experience in the industry, including regulatory filings and 5+ years managing technical professionals.
  • Proficient in drug development, clinical trial methodology, regulatory guidance, and statistical concepts.
  • Broad expertise in statistical programming and clinical data structure.
  • Proficient in SAS and other tools like MS Office, XML, Pinnacle 21.
  • Demonstrated ability to collaborate in a team environment.

Preferred Requirements

  • Membership in industry organizations and presentation experience at Conferences/Congresses.

If you find a role that excites you but you don’t meet every requirement, we encourage you to apply. You may be one step away from a transformative career.

Our Vision: Uniquely Interesting Work, Life-Changing Careers

At Bristol Myers Squibb, our mission is "Transforming patients’ lives through science™". Every employee plays an integral role in our inclusive culture that values passion, innovation, urgency, accountability, inclusion, and integrity. Join our mission today!

On-site Protocol

Bristol Myers Squibb offers diverse work structures:

  • Site-essential roles: Require 100% on-site presence at an assigned facility.
  • Site-by-design roles: Eligible for hybrid work with at least 50% on-site presence.
  • Field-based and remote-by-design roles: Require travel for customer, patient, or business partner engagements as directed.

We are committed to supporting employees with disabilities, ensuring a transparent recruitment process and reasonable accommodations. If you need accommodations during the application or recruitment process, please contact adastaff