Director Integrated Data Quality

About the Role

Provide strategic leadership for the development, implementation, and continuous improvement of integrated data review processes across clinical programs. In partnership with Biostatistics and cross-functional collaborators, establish scalable frameworks, standards, and oversight models to enable proactive, risk-based identification of data issues and ensure high-quality, inspection-ready clinical data. Drive consistent execution of Data Review Plans and promote adoption of integrated data review practices across study teams.

Responsibilities

• Define and lead the Integrated Data Review (IDR) strategy, including the implementation of an appropriate operating model and governance framework across the portfolio.
• Accountable for consistent execution, oversight, and critical issue resolution of Data Review Plans (DRPs), and proactive identification of data quality risks.
• Define minimum requirements and develop standardized data review plan methodologies, templates, processes, and guidance to enable consistent and effective execution across study teams.
• Provide oversight of data review plan execution through established governance processes, KPIs, and quality metrics to ensure consistency, effectiveness, adherence to standards, and continuous improvement across programs.
• Partner with the Clinical Data Reporting group to develop, implement, and maintain standardized libraries of data review outputs, including visualizations, listings, dashboards, and patient profiles, that support scalable and consistent execution of integrated data review processes across programs.
• Collaborate with Quantitative Innovation and Statistical Strategy (QISS) team to translate Risk-Based Data Management (RBDM) methodologies into practical data review approaches and study-level requirements.
• Proactively identify potential risks to data quality, integrity, and delivery timelines and implement mitigation strategies to ensure continuity, compliance, and successful delivery of departmental objectives.
• Drive continuous improvement and innovation in IDR methodologies and technologies through analysis of metrics, lessons learned, inspection observations, and evolving industry practices.
• Develop and maintain SOPs, work instructions, templates, and training materials using quality-by-design principles to support integrated data review processes.
• Lead implementation, change management, and training initiatives to ensure consistent adoption.
• Drive adoption of IDR methodologies across clinical and external data domains to support proactive issue detection and improved data quality outcomes.
• Liaise with internal and external collaborators to develop strong relationships and ensure effective cross-functional collaboration and communication with respect to deliverables and throughout the drug development process.

Requirements

• 12+ years in Clinical Data Management within the biotechnology, pharmaceutical, or health-related industry.
• 5+ years of people management, leadership, and mentoring experience.
• Expert knowledge of clinical data management principles, processes, technologies, and industry best practices.
• Expert knowledge of integrated data review principles, data quality management, and critical-to-quality concepts.
• Deep understanding of regulatory requirements and industry standards, including ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, and global data privacy regulations, with the ability to apply these in an operational setting.
• Working knowledge of RBDM principles and their application to Integrated Data Review, including centralized monitoring activities.
• Understanding of Risk-Based Quality Management (RBQM) principles and their relationship to integrated data review and centralized monitoring.
• Demonstrated experience establishing, implementing, and evolving integrated data review frameworks, governance models, and methodologies across clinical programs.
• Experience identifying critical data and defining risk-based data review strategies.
• Experience interpreting and analyzing clinical, operational, and external data to identify data trends and potential quality issues.
• Experience developing, implementing, and overseeing Data Review Plans and associated governance processes.
• Demonstrated ability to partner with cross-functional collaborators to support risk-based and integrated data review approaches.
• Understanding of KPIs and quality metrics used to assess effectiveness and impact of integrated data review activities.
• Demonstrated success in solving complex business problems through strategic and critical thinking.
• Proven ability to lead and influence within a matrix organization, driving alignment and outcomes across cross-functional stakeholders without direct authority.

Location & Schedule

Locations: Warren, NJ; Armonk, NY; Tarrytown, NY

Work model: On-site 4 days a week

Travel percentage: 10%

Pay

Salary Range (annually): $183,100.00 - $305,200.00

Benefits

Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:

• Annual bonuses or other incentive plans
• Equity awards
• Pension or retirement benefits, 401(k) company match
• Health and wellness programs, fitness centers
• Insurance benefits (e.g., medical, dental, vision, life, and disability)
• Paid time off
• Family support benefits