Director Program Operations Leader

Regeneron Pharmaceuticals; Armonk (NY); Hybrid; USD 205,000 - 342,000; Full time

Benefits offered by this job

Hybrid work model

Job summary

Regeneron Pharmaceuticals, a leader in biotech, seeks a Director to manage Clinical Trial Management Program Operations in a hybrid US-based role. You will orchestrate complex programs, coordinate senior stakeholders, and drive budgets, timelines, and vendor partnerships to ensure study success.

Responsibilities include leading cross-functional study teams, forecasting resources, and supporting regulatory readiness.

Qualifications

• Bachelor’s degree required; advanced degree may be considered in lieu of experience.
• Minimum 12 years in clinical operations or related fields.
• Knowledge of ICH/GCP and SOPs.

Responsibilities

• Lead operational strategy and delivery for complex clinical programs.
• Oversee program quality, timelines, budgets, and study team success.
• Provide input on feasibility, timelines, and cost estimates.
• Review plans during protocol design, startup, and conduct.
• Manage vendor selection, CRO oversight, and governance meetings.
• Ensure inspection readiness and support for regulatory inspections.

Skills

Strategic leadership

Program delivery

Budget management

Vendor management

CRO oversight

Regulatory inspection readiness

Staff recruitment and coaching

Communication with senior management

Education

Bachelor’s degree

Advanced degree preferred

Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director Clinical Trial Management Program Operations Leader to join our Clinical Trial Management team, supporting our clinical development organization in a hybrid work mode. In this role, you will lead operational strategy and delivery for complex clinical programs while collaborating with senior leaders, vendors, collaboration partners, and clinical 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:

US - Armonk, Warren or Cambridge - Hybrid (3 days in the office)

Discover your role:

• Lead operational strategy and overall delivery for complex clinical programs.

• Oversee program quality, timelines, budgets, and study team success.

• Provide operational input to Clinical Study Concepts, feasibility, timelines, and cost estimates.

• Review plans during protocol design, study startup, and study conduct.

• Drive decisions, monitor KPIs, and implement risk mitigation strategies.

• Lead vendor selection, CRO oversight, governance activities, and partner meetings.

• Ensure inspection readiness and lead cross-functional support for Regulatory Authority inspections.

• You bring an innovative approach to solving operational challenges and advancing guidelines.

This role requires:

• Bachelor’s degree.

• Advanced degree may be considered in lieu of proven experience.

• Minimum 12 years of relevant proven experience.

• Minimum 8 years of experience within clinical operations.

• Knowledge of applicable regulations, International Council for Harmonisation/Good Clinical Practice (ICH/GCP), and SOPs.

• Experience leading complex clinical programs and handling operational strategy, budgets, timelines, and resources.

• Experience forecasting and allocating Clinical Trial Management resources across programs.

• Experience managing Clinical Research Organizations (CROs), vendors, and external partners.

• Experience representing Clinical Trial Management at review committees and governance meetings.

• Experience leading staff recruitment, performance management, development, coaching, mentoring, training, and compliance activities.

• Ability to communicate effectively with senior management, partners, and cross-functional teams.

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.

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)

$205,000.00 - $341,600.00