Senior Biostatistician — Oncology Trials | Flexible Hours

Theradex Oncology

Princeton (NJ)

On-site

USD 130,000 - 160,000

Full time

14 days+
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Benefits offered by this job

Medical, dental, vision plans
401(k) matching
Tuition reimbursement
Generous vacation/sick leave
Flexible work schedules

Job summary

Theradex Oncology is seeking a senior biostatistician to lead statistical deliverables across oncology trials. You will write and review SAPs, assist in protocol design, and generate SAS analyses while ensuring quality and regulatory compliance.

The role requires a Master’s in Biostatistics and 5+ years in clinical biostatistics within a CRO/pharma setting, with oncology trial experience preferred. Strong communication and project management skills are essential.

Qualifications

  • Master’s degree in Biostatistics or equivalent is required.
  • 5+ years of experience in clinical biostatistics is required.
  • CRO/pharmaceutical environment experience preferred.
  • Oncology trials experience preferred.

Responsibilities

  • Ensure high-quality statistical deliverables.
  • Write/review SAPs (Statistical Analysis Plans).
  • Design protocol studies and determine sample sizes.
  • Write TLF (Tables, Listings, Figures) plans.
  • Review CRFs and randomization/blinding plans.
  • Develop/validate SAS code for analyses.
  • Maintain study documentation and CSR reviews.
  • Stay current with statistical literature and methods.

Skills

Statistical design
Drug development
Communication
Project management
Risk assessment
Time management
SOP knowledge
FDA/ICH guidelines

Education

Master’s degree in Biostatistics or equivalent

Tools

MS Office
Outlook

Job description

Theradex Oncology is seeking a senior biostatistician to lead statistical deliverables across oncology trials. You will write and review SAPs, assist in protocol design, and generate SAS analyses while ensuring quality and regulatory compliance.

The role requires a Master’s in Biostatistics and 5+ years in clinical biostatistics within a CRO/pharma setting, with oncology trial experience preferred. Strong communication and project management skills are essential.

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