Senior Biostatistician

Theradex OncologyPrinceton, NJ

About The Position

As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.

Requirements

  • Master’s degree in Biostatistics or equivalent, required
  • 5+ years of experience in clinical biostatistics, required
  • Prior experience in a CRO/pharmaceutical environment, required
  • Expertise in statistical concepts and design
  • Understands the investigational drug development process
  • Demonstrates ability to build and maintain effective relationships with others
  • Strong communication, organizational and decision-making skills
  • High level of agility and diplomacy
  • Must be able to anticipate challenges and project risks and proactively implement solutions
  • Strong time management and effective planning skills
  • Knowledge of Standard Operating Procedures
  • Working knowledge of FDA and ICH guidelines
  • Working knowledge of MS Office and Outlook

Nice To Haves

  • Oncology clinical trials preferred
  • Experience with phase I trials preferred

Responsibilities

  • Ensures successful completion of high-quality statistical deliverables
  • Writes and/or reviews statistical sections of protocols
  • Assists in protocol study design (determines sample sizes for all phases of trials)
  • Writes Statistical Analysis Plans (SAPs)
  • Writes Tables, Listings and Figures Plans (TLF Plans)
  • Reviews and/or designs Case Report Forms (CRFs)
  • Reviews and/or writes randomization and blinding plans
  • Reviews and/or writes charters for Data Monitoring Committees (DMCs)
  • Provides SAS code for statistical models
  • Validates/performs SAS programming for key data analyses
  • Performs quality control on derived variables being analyzed
  • Interprets results from analysis
  • Maintains documentation
  • Reviews Clinical Study Reports (CSR)
  • Keeps abreast of statistical literature/design
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