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Biostatistician - IV - Job Opportunity at Binding Minds Inc.

Remote, US
Contract
Senior
Posted: March 16, 2025
Remote
USD 166,400-176,800 per year

Benefits

Remote work flexibility
Independent work environment
Professional development through complex project exposure
Direct interaction with global health authorities
Strategic role in drug development

Key Responsibilities

Lead statistical design and analysis for complex clinical studies
Contribute to global drug development strategy and regulatory submissions
Guide and oversee CRO teams for statistical analysis
Develop and validate statistical analysis plans and protocols
Interface with cross-functional study teams and health authorities
Ensure data quality and regulatory compliance
Drive post-hoc analysis initiatives

Requirements

Education

MS or PhD in statistics or biostatistics

Experience

5+ years pharmaceutical experience with 2-3 years Oncology experience (Phases 2 to Phase IV)

Required Skills

Advanced SAS and/or R programming nQuery and East software proficiency Statistical methodology expertise Clinical trial methodology knowledge Strong analytical and problem-solving abilities Project management and vendor oversight Excellent oral and written communication
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Sauge AI Market Intelligence

Industry Trends

Increasing focus on real-world evidence and adaptive trial designs in oncology research has elevated the importance of sophisticated statistical expertise Growing complexity in clinical trial designs, especially in oncology, requires advanced post-hoc analysis capabilities Rising demand for biostatisticians who can bridge technical expertise with strategic drug development insights Trend toward decentralized clinical trials is creating new statistical challenges and opportunities

Salary Evaluation

Market rate for senior biostatisticians in pharma ranges from USD 150,000 to 190,000 annually, with contract rates typically commanding a premium

Role Significance

Typically interfaces with 5-10 person core study teams while leading 2-3 CRO statistical teams
Senior individual contributor role with significant strategic input into drug development and trial design

Key Projects

Phase II-IV oncology clinical trials Regulatory submission preparation Post-hoc analysis for publication support Protocol development and optimization Statistical analysis strategy development

Success Factors

Ability to balance statistical rigor with practical drug development needs Strong understanding of regulatory requirements across global markets Excellence in translating complex statistical concepts to non-technical stakeholders Proactive problem-solving and issue identification Effective management of CRO relationships and deliverables

Market Demand

Very high demand, particularly for oncology experience combined with advanced statistical expertise

Important Skills

Critical Skills

Advanced statistical methodology expertise especially in oncology trials Strong programming skills in SAS/R for complex analysis Strategic thinking in trial design and analysis Regulatory knowledge and health authority interaction experience

Beneficial Skills

Machine learning and adaptive trial design expertise Experience with specialized oncology endpoints Knowledge of emerging statistical methodologies Experience with real-world evidence analysis

Unique Aspects

High level of independence in statistical decision-making
Direct involvement in strategic drug development planning
Significant interaction with global health authorities
Focus on complex oncology trials

Career Growth

2-3 years in role typically required before advancement to principal or director level positions

Potential Next Roles

Principal Biostatistician Statistical Science Director Global Head of Biostatistics Clinical Development Strategy Leader

Company Overview

Binding Minds Inc.

Contract research and consulting organization specializing in clinical development support

Mid-sized player in the clinical research support sector
US-based with global project scope
Results-driven environment with emphasis on independent work and technical expertise
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