Regeneron Pharmaceuticals, Inc (USA) Posted October 13, 2026

Associate Director, Digital Health Technologies

Warren, United States Full time
Clinical Development Associate Director
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Regeneron Pharmaceuticals, Inc (USA) is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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: Warren, NJ

May 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

This role requires:

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:

Education: Bachelor’s degree required; MBA preferred

Experience: Minimum of 10 years of relevant industry experience

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 https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . 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

Job details

Seniority
Associate Director
Function
Clinical Development
Therapeutic area
Not listed
Location
Warren, United States
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 567 comparable Associate Director Clinical Development roles across 75 biopharma companies.

567Comparable roles tracked
504Currently active
75Companies hiring similar roles
46Countries represented

Salary context

173 of 567 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $157,200/yr – $256,600/yr
Lowest disclosed · Sr Site Activation Coordinator · IQVIA $35,800/yr – $102,000/yr
Highest disclosed · Sr Statistical Advisor · Gilead Sciences, Inc. $261,375/yr – $338,250/yr
Peer group range $68,900 – $299,813 (median $176,800)

Where these roles are based

Top locations among the 567 comparable roles

United States245
India70
United Kingdom36
Spain22
China18
Poland18

+ 40 more countries

Seniority mix

567 of 567 peers have a known seniority level

Manager288
Senior149
Associate Director130

Therapeutic area mix

51 of 567 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology28
Immunology8
Neuroscience6
Respiratory2
Ophthalmology2
Gastroenterology2
Dermatology & Aesthetics2
Cardiovascular / CVRM1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
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Notify me about similar jobs

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.