What are the responsibilities and job description for the Associate Director, Data Validation Strategy position at Regeneron Pharmaceutical?
Build our future together
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Data Validation Strategy join our Clinical Data Management organization, leading the strategy and execution of integrated data review, helping ensure our clinical data is high-quality and inspection-ready. You will collaborate with Biostatistics, Clinical Data Reporting, Quantitative Innovation and Statistical Strategy (QISS), and study teams.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where
Location: Warren, NJ, Armonk or Tarrytown, NY
Work model: Primarily on-site with hybrid flexibility
Travel percentage: Up to 25%
Discover your role
Lead the implementation and execution of the Integrated Data Review (IDR) strategy, operating model, standards, and governance
Oversee the development, execution, and quality of Data Review Plans (DRPs), including issue tracking, escalation, and resolution
Partner with Biostatistics, QISS, Clinical Data Reporting, and study teams delivering risk-based data review aligned with critical-to-quality factors
Monitor performance through KPIs and quality metrics to identify trends and drive continuous improvement
Support the development of SOPs, work instructions, templates, and training materials for IDR activities
Lead training, coaching, and change management to drive adoption of IDR across clinical and external data domains
Drive innovation, automation, and AI-enabled analytics initiatives
Manage, mentor, and develop the Integrated Data Review and Quality team
This role requires
Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related field
10 years of Clinical Data Management experience within the biotechnology, pharmaceutical, or healthcare industry and 5 years of people, team, and project leadership experience
Experience implementing integrated data review, quality management, risk-based data management, or centralized review processes
Strong working knowledge of ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, and RBDM/RBQM principles
Experience supporting inspection readiness activities
Experience with data review tools, visualization, and analytics for proactive issue detection
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or 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, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.
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.
Salary Range (annually)
$157,200.00 - $256,600.00
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Data Validation Strategy join our Clinical Data Management organization, leading the strategy and execution of integrated data review, helping ensure our clinical data is high-quality and inspection-ready. You will collaborate with Biostatistics, Clinical Data Reporting, Quantitative Innovation and Statistical Strategy (QISS), and study teams.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where
Location: Warren, NJ, Armonk or Tarrytown, NY
Work model: Primarily on-site with hybrid flexibility
Travel percentage: Up to 25%
Discover your role
Lead the implementation and execution of the Integrated Data Review (IDR) strategy, operating model, standards, and governance
Oversee the development, execution, and quality of Data Review Plans (DRPs), including issue tracking, escalation, and resolution
Partner with Biostatistics, QISS, Clinical Data Reporting, and study teams delivering risk-based data review aligned with critical-to-quality factors
Monitor performance through KPIs and quality metrics to identify trends and drive continuous improvement
Support the development of SOPs, work instructions, templates, and training materials for IDR activities
Lead training, coaching, and change management to drive adoption of IDR across clinical and external data domains
Drive innovation, automation, and AI-enabled analytics initiatives
Manage, mentor, and develop the Integrated Data Review and Quality team
This role requires
Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related field
10 years of Clinical Data Management experience within the biotechnology, pharmaceutical, or healthcare industry and 5 years of people, team, and project leadership experience
Experience implementing integrated data review, quality management, risk-based data management, or centralized review processes
Strong working knowledge of ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, and RBDM/RBQM principles
Experience supporting inspection readiness activities
Experience with data review tools, visualization, and analytics for proactive issue detection
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or 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, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.
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.
Salary Range (annually)
$157,200.00 - $256,600.00
Salary : $157,200 - $256,600