Global Site Start-Up Leader – Clinical Trials

Regeneron Pharmaceuticals, Inc.; Armonk (NY); On-site; USD 140,000 - 200,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Manager, Global Site Start-Up Lead (SSU Lead) based in Armonk, NY, with responsibility for driving global site activation for clinical trials.

You will balance strategic oversight with hands‑on leadership, partnering with cross‑functional teams and CROs to ensure timely site activation, risk mitigation, and compliant documentation across trials. You will develop projections, track milestones, and monitor CRO performance using metrics.

Qualifications

• Interpersonal and leadership skills for cross‑functional collaboration.
• Ability to understand and implement operational strategic direction for clinical studies.
• Data-driven approach to planning, executing, and problem solving.
• Effective communication skills in verbal, written, and presentation formats.
• Proactive, disciplined, and able to meet deadlines and prioritize tasks.
• Ability to influence and negotiate with key stakeholders.
• Experience in the clinical drug development process with site start‑up expertise.
• Vendor management experience.

Responsibilities

• Develop the site start-up strategy for each study and outline dependencies.
• Oversee tracking and analysis of study metrics to evaluate CRO performance and drive corrective actions.
• Advocate for optimized site selection using data-driven insights.
• Lead development and alignment of site activation projections with cross-functional teams and CROs.
• Ensure compliant TMF documentation and inspection readiness.

Skills

Leadership

Cross-functional

Data-driven

Regulatory knowledge

Vendor management

Tools

CTMS

TMF

MS Office

Job description

Regeneron Pharmaceuticals, Inc. is seeking a Manager, Global Site Start-Up Lead (SSU Lead) based in Armonk, NY, with responsibility for driving global site activation for clinical trials.

You will balance strategic oversight with hands‑on leadership, partnering with cross‑functional teams and CROs to ensure timely site activation, risk mitigation, and compliant documentation across trials. You will develop projections, track milestones, and monitor CRO performance using metrics.