Senior Biostatistician

SB_4237666295
  • United States (Remote)
  • Contract

Are you a seasoned biostatistician with a passion for oncology and innovation?


Do you enjoy turning complex data into strategic clinical insights?


Looking for a flexible, remote role where your expertise truly shapes drug development?


If so, this opportunity may be exactly what you're looking for.


We’re seeking an experienced Biostatistician to play a pivotal role in shaping clinical development strategies. This is a remote, flexible position (30–40 hours/week) with core collaboration hours between 9 AM–3 PM EST.


What You'll Do

  • Provide expert statistical input into clinical development plans, protocols, analysis plans, and regulatory submissions
  • Interpret complex data and translate it into actionable clinical and regulatory insights
  • Partner cross-functionally with clinical research, regulatory, data management, programming, and medical writing teams
  • Support publications and scientific presentations as the internal statistical lead
  • Champion innovative statistical methods to streamline development and enhance decision-making


What You Bring

  • 10+ years (MS) or 7+ years (PhD) of experience in clinical drug development
  • Strong background in oncology (solid tumours or hematologic malignancies)
  • Proven track record with NDA/BLA submissions is a plus
  • Proficiency in SAS, R, and other statistical programming tools
  • In-depth knowledge of FDA/ICH guidelines, CDISC standards, and global regulatory expectations
  • Strong communication skills, critical thinking, and collaborative spirit
  • Desire to thrive in a fast-paced, forward-thinking environment


Education

MS or PhD in Statistics, Biostatistics, Mathematics, or a related field


Ready to apply your expertise where it truly matters?


We’d love to hear from you. Reach out to learn more or apply today.

Lavina Rose Associate Director / AVP

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