Associate Director, Digital Health Technologies

Regeneron Pharmaceuticals Inc.; Warren Township (NJ); On-site; USD 157,000 - 257,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

401(k) company match

Health and wellness programs

Paid time off

Job summary

Regeneron Pharmaceuticals Inc. invites a senior leader to oversee digital health and COA program strategy, driving cross-functional collaboration and ensuring data quality across studies.

You will manage vendor relationships, budgets, and regulatory compliance while guiding eCOA and DHT activities with innovative approaches. Ideal candidates bring 10+ years in clinical development with leadership experience, MBA preferred, and a proven track record of delivering compliant, timely program results

Qualifications

• Minimum 10 years in clinical development or digital health contexts.
• Experience leading COA/DHT programs and vendor governance.
• Proven ability to manage budgets, timelines, and regulatory expectations.

Responsibilities

• Lead COA/DHT strategy and development across programs.
• Oversee vendor onboarding, contracts, and performance metrics.
• Ensure regulatory compliance and data quality across studies.

Skills

Strategic program management

Cross-functional leadership

Vendor management

Budget management

Regulatory compliance (GCP/ICH)

Team leadership

Education

Bachelor’s degree

MBA preferred

Job description

Build our future together: The Associate Director – Digital Health Technology (DHT) leads the strategic management of one or more COA (Clinical Outcome Assessment) and DHT programs. This individual owns operational decisions — instrument selection, validation, debriefing, translation, DHT planning, vendor onboarding and oversight, quality, timelines, and budgets — for COA and DHT activities within assigned programs, in accordance with applicable regulations, ICH/GCP standards, and company SOPs. The role serves as a cross-functional liaison, raising awareness of Regeneron-specific COA/DHT/data integration needs, and provides oversight at both the clinical development unit/program level and the individual study level for eCOA and DHT technologies (e.g., wearables, sensors, ECG, spirometry). As the Subject Matter Expert, this person advises study teams on best practices to ensure regulatory compliance and data quality, manages vendor performance at the program level, and holds line management responsibility for staff recruitment, development, coaching, mentoring, and performance management.

When & where:

• Primary Location: Tarrytown, NYMay require up to 25% travel

Discover your role: Program & Study Oversight

• Accountable for the successful, compliant delivery of eCOA and DHT (wearables, sensors, ECG, spirometry) across assigned clinical programs
• Executes the COA/DHT development process — study design, execution, change control, and database lock activities
• Owns the overall success of COA/DHT development and strategy within assigned clinical development unit(s)/program(s)
• Maintains visibility into program status and issues; proactively communicates progress, risks, and changes affecting quality, timelines, or budget
• Reviews key metrics and KPIs across studies to track progress and vendor performance
• Ensures inspection readiness throughout the clinical program lifecycle

Planning & Setup

• Leads the Program Planning and Setup phases of eCOA/DHT, including:
• Guiding COA/DHT and digital endpoint selection through team collaboration and literature review
• Supporting Health Economics Outcomes Research (HEOR) with instrument development
• Overseeing cognitive debriefing, psychometric validation studies, and DHT verification, validation, and usability activities
• Provides input during protocol development to ensure consistency across the program
• Provides operational insight into COA/DHT selection, vendor options, timelines, and cost estimates during program/study development

Vendor Management

• May own vendor relationship management, including:
• Vendor selection and maintenance
• Participation in vendor governance/oversight meetings
• Review, negotiation, and standardization of vendor contracts and budgets with procurement
• Establishing vendor performance metrics and reviews
• Delivering standard vendor/sponsor expectations and operational processes
• Acting as the point of contact for trial-specific and vendor-related escalations, ensuring preventative actions are implemented
• Participates in eCOA, DHT, and translation vendor governance meetings as needed

Problem Solving & Risk Management

• Applies problem-solving strategies and maintains issue-tracking documentation to monitor progress and ensure timely resolution
• Proactively creates and implements risk mitigation strategies
• Provides innovative, flexible COA/DHT solutions and scenario planning for cross-functional teams
• Drives decision-making by integrating all COA/DHT operational considerations to ensure program goals are attainable before implementation
• Acts as the point of contact for program- and study-level escalations

Resourcing & Continuous Improvement

• Responsible for COA/DHT resource forecasting and allocation across clinical studies/programs
• Identifies and recommends changes to practices and policies; initiates and participates in strategic and continuous improvement projects within Global Development
• Utilizes AI as applicable to improve quality, efficiency, and effectiveness of process and product development

People Leadership

• Directly supervises COA/DHT staff, including work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training/compliance, and study support oversight

Knowledge & Technical Skills

• Demonstrated knowledge of COA and DHT systems development processes, including wearables, sensors, ECG, and spirometry
• Understanding of relevant industry trends in digital health technologies and digital endpoints
• Ability to apply AI and automation to improve DHT/eCOA processes and products
• Working knowledge of GCP and ICH guidelines
• Extensive experience in global clinical trial operations

Leadership & Interpersonal Skills

• Strong interpersonal and leadership skills
• Ability to provide strategic direction and guidance for clinical programs
• Ability to influence and negotiate
• Ability to build productive teams and collaborations
• Line management experience with demonstrated mentoring and coaching skills

Operational & Analytical Skills

• Analytical, data-driven approach to planning, executing, and problem-solving
• Strong project management, cross-functional leadership, and organizational skills
• Budget management experience
• Demonstrated vendor management experience
• Effective communication skills — verbal, written, and presentation

Work Style

• Proactive and self-disciplined; able to meet deadlines, manage time effectively, and prioritize

Education: Bachelor’s degree required; MBA preferred

Experience: Minimum of 10 years of relevant industry experience

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 https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process.

Benefits

• 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

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

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.