Hybrid Clinical Supply Operations Specialist

Regeneron Pharmaceuticals; Dublin; Hybrid; EUR 46,000 - 75,000; Full time

Job summary

Regeneron Pharmaceuticals seeks a Clinical Supply Operations Specialist to support the Clinical Drug Supply & Logistics team in a hybrid Dublin role. You will manage investigational product supply, inventory planning and documentation across multiple therapeutic areas, coordinating with QA, regulatory and external stakeholders to ensure uninterrupted study conduct.

The role requires 2+ years in Clinical Supplies or related fields, knowledge of ICH/GCP, and experience with distribution,

Qualifications

• 2+ years of experience in Clinical Supplies or related field.
• Fundamental knowledge of the clinical drug development process and GCP guidelines.
• Experience supporting investigational product distribution, inventory planning and accountability.
• Familiarity with IRT management activities and UAT/testing.
• Strong documentation and regulatory-compliance skills.
• Ability to work in a cross-functional, fast-paced environment.

Responsibilities

• Manage investigational product supply and inventory planning for moderately sophisticated clinical studies.
• Coordinate accountability, reconciliation, returns and destruction activities with accurate records.
• Oversee internal system management including lot creation, batch status updates, and shipment execution.
• Supervise supply risks, depot stocking levels, inventory trends and temperature excursions.
• Support eTMF activities, document lists, and regulatory-compliant management.
• Coordinate QA/QP release activities, pack-and-label reconciliation and inspection readiness.
• Support ancillary supply planning, procurement, inventory management and logistics.

Skills

Clinical supplies

Regulatory knowledge

Quality Assurance

IRT management

Inventory planning

Education

BS/BA degree in related field

Tools

eTMF systems

IRT tools

Job description

Regeneron Pharmaceuticals seeks a Clinical Supply Operations Specialist to support the Clinical Drug Supply & Logistics team in a hybrid Dublin role. You will manage investigational product supply, inventory planning and documentation across multiple therapeutic areas, coordinating with QA, regulatory and external stakeholders to ensure uninterrupted study conduct.

The role requires 2+ years in Clinical Supplies or related fields, knowledge of ICH/GCP, and experience with distribution,