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Associate Director, Biostatistics

Job in Princeton, Mercer County, New Jersey, 08543, USA
Listing for: Scorpion Therapeutics
Full Time position
Listed on 2026-08-30
Job specializations:
  • Science
    Clinical Research, Research Scientist
Salary/Wage Range or Industry Benchmark: 189670 - 229834 USD Yearly USD 189670.00 229834.00 YEAR
Job Description & How to Apply Below

Position Summary

  • Associate Director of Biostatistics on cross-functional Development teams; contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. May support a particular indication/asset.
Key Responsibilities
  • Collaborate on innovative, efficient clinical trial design (population/endpoints) and project development strategy.
  • Defend protocols and analysis plans at internal governance reviews; independently review complex protocols.
  • Author and/or review protocols, statistical analysis plans, clinical study reports, publications, and other study-level documents.
  • Present analyses and summary data clearly and transparently.
  • Provide statistical support/leadership for health authority requests and public release (publications/presentations).
  • Manage multiple studies ensuring standards and consistency within an indication/therapeutic area.
  • Apply statistical/clinical trials methodology to clinical development; partner on drug development as a matrix team member.
  • Ensure compliance with BMS processes/SOPs and quality of deliverables.
  • Contribute to statistical community of practice; develop/advice team members.
  • (People manager) Advocate for employees; coach/mentor; lead to empower/develop team; guide development plans; performance reviews/metrics.
Qualifications & Required/Preferred Skills
  • PhD with 6+ years’ experience or MS with 8+ years in statistics/biostatistics (or related) with clinical trials/drug development/pharma/healthcare.
  • Proficiency in SAS, R, or Python; implement advanced statistical analysis, data manipulation, graphing & simulation.
  • Strong interpersonal, communication, writing, organizational, collaboration, and leadership skills.
  • Expert in statistical/clinical trials methodology; knowledge of regulatory landscape and regulatory interactions.
  • Strong planning/prioritization and project management.
  • People manager experience preferred (for people manager role).
Compensation (FTE)
  • Cambridge Crossing: $218,120–$264,308
  • Princeton, NJ: $189,670–$229,834
  • Seattle, WA: $208,640–$252,824
Benefits (selected)
  • Health Coverage;
    Wellbeing Support; 401(k) and protection benefits (e.g., disability, life insurance).
On-site Protocol
  • Site-essential: 100% onsite;
    Site-by-design: hybrid with at least 50% onsite; field/remote-by-design: ability to travel to visit customers/patients/partners and attend meetings as directed.
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Position Requirements
10+ Years work experience
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