Hybrid IRT & Clinical Supply Systems Lead

Regeneron Pharmaceuticals; Uxbridge; Hybride; GBP 87 000 - 142 000; Plein temps

Résumé du poste

Regeneron Pharmaceuticals is seeking a Clinical Supply Systems Manager to support IRT systems within our Clinical Supply Systems Group, enabling robust management of clinical trials in a hybrid work setting. You will collaborate with clinical trial management, data management, biostatistics and clinical supply leads to ensure smooth system deployments and study execution.

The role requires a Bachelor’s degree or eight years’ equivalent experience, with four years in biotech/pharma and two years

Qualifications

• Bachelor’s degree or eight years’ equivalent experience.
• Four years’ biotechnology/pharmaceutical experience, including two with IRT systems.
• IRT development experience, protocol interpretation and IRT terminology knowledge.
• ICH/GCP and regulatory guidelines knowledge.
• Proficiency in Microsoft Office Suite.

Responsabilités

• Lead IRT study-team support from protocol-aligned requirements through conduct and closeout.
• Oversee vendor functionality, processes and performance through issue-resolution and risk-management meetings.
• Manage deployment timelines and application launches with internal teams and vendors.
• Maintain requirements, user guides, training materials and communication plans.
• Coordinate user acceptance testing.
• Coordinate randomisation and kit-list uploads with Clinical Logistics and biostatistics.
• Develop vendor-supported clinical-team and site training for investigators or CRAs.

Connaissances

IRT systems

Leadership

Project management

Cross-functional collaboration

Microsoft Office

Formation

Bachelor's degree or equivalent experience

Outils

Microsoft Office

Description du poste

Regeneron Pharmaceuticals is seeking a Clinical Supply Systems Manager to support IRT systems within our Clinical Supply Systems Group, enabling robust management of clinical trials in a hybrid work setting. You will collaborate with clinical trial management, data management, biostatistics and clinical supply leads to ensure smooth system deployments and study execution.

The role requires a Bachelor’s degree or eight years’ equivalent experience, with four years in biotech/pharma and two years