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Director, Statistical Programming, TMTT - Job Opportunity at Edwards Lifesciences

Seattle, USA
Full-time
Executive
Posted: January 19, 2025
Remote
USD 177,000 - 251,000 per year

Benefits

Competitive performance-based incentives
Comprehensive benefits package tailored to individual needs
Career development and mentorship opportunities
Work in cutting-edge medical technology sector

Key Responsibilities

Lead and oversee statistical programming teams for clinical studies
Perform senior review of SAS outputs and ensure quality deliverables
Manage talent development including hiring, training and succession planning
Develop and maintain SAS programs for statistical analysis
Review and validate analysis dataset specifications
Ensure regulatory compliance in programming outputs
Direct resource allocation and project prioritization

Requirements

Education

Master's Degree in Computer Science, Statistics or related fields

Experience

11 years SAS programming experience in pharmaceutical/medical device industry, 3 years managing statistical programmers

Required Skills

Advanced SAS programming Windows operating systems Clinical data analysis Leadership and team management Oral and written communication Project management
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Sauge AI Market Intelligence

Industry Trends

Growing demand for statistical programming expertise in medical device clinical trials Increasing focus on real-world evidence and complex data analysis in cardiovascular treatments Shift towards remote-first technical leadership roles in healthcare

Salary Evaluation

The offered salary range is competitive for director-level statistical programming roles, particularly in the medical device sector. The upper range of $251,000 reflects the strategic importance of data analysis in clinical research.

Role Significance

Typically managing 8-12 statistical programmers across multiple clinical studies
Director-level position with significant influence on clinical trial outcomes and regulatory submissions

Key Projects

Large-scale clinical trials for transcatheter therapies Regulatory submission programming support Statistical analysis system architecture design Clinical evidence generation programs

Success Factors

Strong balance of technical expertise and leadership skills Deep understanding of regulatory requirements in medical device clinical trials Ability to translate complex statistical requirements into programming frameworks Experience with cardiovascular medical devices preferred

Market Demand

Very high demand due to increasing complexity of clinical trials and emphasis on data-driven decision making in medical device development

Important Skills

Critical Skills

Advanced SAS programming expertise crucial for complex clinical trial analysis Leadership skills essential for team development and project success Regulatory knowledge critical for compliance

Beneficial Skills

Experience with emerging statistical software platforms Knowledge of cardiovascular medical devices Understanding of global regulatory requirements

Unique Aspects

Focus on transformative heart valve technologies
Direct impact on patient outcomes through statistical analysis
Combination of technical leadership and clinical research expertise

Career Growth

Typical progression to next level within 3-5 years based on business impact and strategic contributions

Potential Next Roles

Senior Director of Biometrics VP of Clinical Data Sciences Global Head of Statistical Programming

Company Overview

Edwards Lifesciences

Edwards Lifesciences is a global leader in patient-focused medical innovations for structural heart disease and critical care monitoring

Industry leader in transcatheter heart valve technology with strong market position in structural heart treatments
Major presence in Seattle tech hub with significant R&D investment
Innovation-driven environment with strong focus on patient outcomes and clinical excellence
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