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Key Responsibilities:

  • Serve as study biostatistician across development programs, authoring Statistical Analysis Plans and overseeing TFL generation.
  • Plan and implement statistical analyses for clinical study reports and regulatory submissions.
  • Contribute to innovative trial designs, simulations, and process improvements.

Requirements:

  • PhD in Statistics/Biostatistics with 5+ years of experience or Master’s with 10+ years.
  • Strong knowledge of clinical development and statistical analysis principles.
  • Proficiency in SAS and R; experience with NDA/BLA submissions preferred.

Benefits:

  • Remote/hybrid work flexibility and global exposure across clinical programs.
  • Opportunities for professional growth, learning, and technical capability building.
  • Competitive salary, healthcare, paid leave, and retirement benefits.

Partner Company

The partner company specializes in global clinical development, supporting registration-directed clinical trials across therapeutic areas. It fosters a collaborative, results-oriented culture with a focus on innovation, professional growth, and high-quality deliverables.

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