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Principal Statistical Programmer - Job Opportunity at TK-CHAIN LLC

Princeton, United States
Full-time
Senior
Posted: May 4, 2025
On-site
USD 140,000 - 180,000 per year based on Princeton market rates and senior role requirements

Key Responsibilities

Lead end-to-end statistical programming for clinical trials including CDISC dataset creation and complex analysis outputs
Provide strategic project management across multiple therapeutic areas with focus on quality and efficiency
Drive technical standards and SOPs while mentoring junior team members
Coordinate cross-functional collaboration between statistics, data management and clinical teams

Requirements

Education

Bachelor's degree required, Master's preferred in scientific discipline

Experience

9+ years of relevant work experience

Required Skills

Expert knowledge of SAS/Base (macros, arrays, formats, ODS) Expert knowledge of SAS/STAT and SAS/GRAPH Strong analytical skills Strong written and verbal communication skills Proficiency with Word, Excel, and PowerPoint Knowledge of CDISC standards Knowledge of drug development principles Basic statistical principles understanding
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Sauge AI Market Intelligence

Industry Trends

Increasing demand for CDISC expertise as regulatory requirements become more stringent in clinical trials Growing emphasis on real-world evidence analysis requiring advanced statistical programming skills Shift towards cloud-based statistical computing platforms and collaborative programming environments Rising importance of automation and efficiency in clinical data analysis workflows

Role Significance

Typically leads a team of 3-5 statistical programmers while collaborating with broader clinical development team of 15-20 members
Senior leadership position with significant influence on technical standards and project outcomes

Key Projects

Phase III clinical trial data analysis and submission preparation Statistical analysis automation and efficiency initiatives CDISC implementation and compliance projects Cross-therapeutic program standardization efforts

Success Factors

Deep expertise in both technical programming and clinical trial processes Strong project management capabilities with focus on quality and efficiency Excellent cross-functional communication and leadership skills Ability to balance multiple high-priority projects while maintaining attention to detail

Market Demand

High demand with significant growth projected due to expanding clinical trial complexity and increasing regulatory requirements

Important Skills

Critical Skills

Advanced SAS programming expertise is foundational for role success and regulatory compliance CDISC standards knowledge essential for ensuring submission-ready deliverables Project management capabilities critical for coordinating complex clinical trial analyses

Beneficial Skills

Knowledge of emerging clinical data standards and regulations Experience with clinical trial automation tools Understanding of pharmaceutical development process Familiarity with cloud-based computing environments

Unique Aspects

Opportunity to shape technical standards and processes
Direct involvement in critical pharmaceutical development programs
Balance of technical leadership and project management responsibilities

Career Growth

2-4 years in role typically required before advancement to director level, depending on project success and organizational growth

Potential Next Roles

Director of Statistical Programming Head of Biometrics Clinical Development Technology Leader

Company Overview

TK-CHAIN LLC

Mid-sized clinical research organization specializing in pharmaceutical development support

Regional player in the pharmaceutical services sector with potential for growth
Strong presence in the Princeton pharmaceutical corridor with access to major pharmaceutical clients
Professional environment with emphasis on technical excellence and regulatory compliance
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