Associate Director, Biostatistics
Benefits
Unlimited PTO
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About the Role:
- Provide strategic statistical leadership for clinical oncology programs.
- Support studies from early-phase dose optimization through regulatory submissions.
Responsibilities:
- Design and execute clinical trial analyses, author key statistical documents, and ensure regulatory compliance.
- Collaborate with cross-functional teams and manage external vendors to deliver high-quality results.
Requirements:
- Advanced degree in Statistics or Biostatistics with relevant industry experience.
- Proficiency in SAS, R, EAST, and knowledge of CDISC standards.
Benefits:
- Competitive salary, comprehensive healthcare, retirement plans, and flexible time off.
Partner Company
They are a biotechnology company developing innovative cancer therapies, including radiopharmaceutical treatments. The culture emphasizes scientific rigor, collaboration, and meaningful impact in a highly regulated environment.