Director Integrated Data Quality

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 183,000 - 305,000; Full time

Benefits offered by this job

Annual bonus

Equity awards

Pension plan

401(k)

Health benefits

Fitness centers

Insurance coverage

Paid time off

Family support

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Director of Integrated Data Review to provide strategic leadership for scalable IDR frameworks across clinical programs.

You will establish governance, drive proactive data quality risk management, and ensure inspection-ready data through standardized DRPs and dashboards. You will partner with Biostatistics and QISS to translate RBQM into practical data review approaches, oversee SOPs, and lead training initiatives to ensure broad adoption across

Qualifications

• 12+ years in Clinical Data Management within biotechnology, pharmaceutical or health industry.
• 5+ years of people management, leadership, and mentoring.
• 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.
• Understanding regulatory requirements including ICH E6(R3), ICH E8(R1), 21 CFR Part 11, and data privacy regulations.

Responsibilities

• Define and lead the IDR strategy and governance across the portfolio.
• Ensure consistent execution and oversight of Data Review Plans (DRPs).
• Develop standardized methods, templates, and guidance for data review across study teams.
• Provide governance over data review plan execution with KPIs and quality metrics.
• Collaborate with cross-functional teams to implement data review outputs like visualizations, listings, dashboards, and patient profiles.
• Drive continuous improvement and adoption of IDR methodologies across programs.
• Lead change management and training to ensure adoption of IDR practices.

Skills

Clinical Data Management

Leadership

Regulatory knowledge

Data quality

Risk management

Job description

Director, Integrated Data Review

Build our future together: The Director, Integrated Data Review provides 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, this role establishes scalable frameworks, standards, and oversight models to enable proactive, risk-based identification of data issues and ensure high-quality, inspection-ready clinical data. The position drives consistent execution of Data Review Plans and promotes adoption of integrated data review practices across study teams.

When & Where:

Location: Warren NJ, Armonk NY, and TarryTown NY

Work model/flexibility: on site 4 days a week

Travel percentage: 10%

Discover your role:

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 of Data Review Plans (DRPs), and proactive identification of data quality risks. Define minimum requirements and develop standardized data review plans methodologies, templates, processes, and guidance to enable consistent and effective execution across study teams. Provide oversight of data review planes 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 drug development process.

This role requires:

• 12+ years in Clinical Data Management within within the biotechnology, pharmaceutical or health related industry.
• With 5+ years of people management, leadership, and mentoring
• Expert knowledge of clinical data management principles, processes, technologies and industry best practices.
• Expert knowledge of integrated data review principles, data qualitymanagement, 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 Risked 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.

Benefits and compensation

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

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

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

Employment equity statement

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Company information

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.

Recruitment and background check

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications. For jobs in Canada: this posting is for an existing position.