Senior Manager, Clinical Supply Ops & Vendor Excellence

Regeneron Pharmaceuticals, Inc (USA); Kentucky; On-site; USD 134,000 - 219,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

Pension benefits

401(k) match

Health & wellness

Fitness center

Insurance (medical, dental, vision)

Paid time off

Family benefits

Job summary

Regeneron Pharmaceuticals, Inc. in Warren, NJ is seeking a Senior Manager of Clinical Supply Operations to lead clinical supply activities and drive continuous improvements across logistics processes.

You will oversee CSO staff and coordinate with external vendors to ensure compliant, timely delivery of clinical trial supplies. The role demands strong leadership, extensive experience with clinical trials, GCP/ICH knowledge, and a track record in cross‑functional projects.

Qualifications

• Strong Leadership Skills.
• Experience working with external vendors.
• Experience leading cross functional projects/initiatives.
• Effective stakeholder management and negotiation skills.
• Ability to multi-task and adapt to changing priorities.
• Coaching and mentoring others.
• Knowledge of clinical trial methodology and GCP/ICH guidelines.
• Minimum: BS/BA degree in a related field.
• 8+ years of industry/relevant professional experience.

Responsibilities

• Oversee CSO activities and vendor oversight for clinical supply logistics.
• Lead cross-functional initiatives to optimize operational efficiency.
• Mentor and train CSO staff; manage TMF documentation.
• Develop and monitor performance metrics and analytics.

Skills

Leadership

Stakeholder management

Vendor management

Cross-functional collaboration

Coaching/Mentoring

GCP/ICH knowledge

Education

BS/BA degree

Masters/MBA/PharmD preferred

Job description

Regeneron Pharmaceuticals, Inc. in Warren, NJ is seeking a Senior Manager of Clinical Supply Operations to lead clinical supply activities and drive continuous improvements across logistics processes.

You will oversee CSO staff and coordinate with external vendors to ensure compliant, timely delivery of clinical trial supplies. The role demands strong leadership, extensive experience with clinical trials, GCP/ICH knowledge, and a track record in cross‑functional projects.