The Senior Manager in Global Development Quality Management leads quality and compliance efforts across clinical trials, ensuring risk-based quality management. Responsibilities include issue management, audit responses, and providing compliance support to stakeholders while managing GCP-compliant activities and leading risk assessment initiatives.

The Manager, GD Quality Standards & Continuous Improvement will manage the Global Development Quality Management System, oversee quality event portfolios, provide subject matter expertise, and facilitate governance activities to enhance quality standards and compliance. The role requires collaboration with stakeholders to advance process improvements and awareness of quality culture within the organization.

The Associate Director in GPS Standards & Training manages the Pharmacovigilance Quality Management System, ensures compliance with regulatory requirements, develops training programs, reviews procedures, monitors training compliance, and leads initiatives to improve GPS processes.

The Director of Program Operations Leader is responsible for leading complex programs in Clinical Trial Management, overseeing all clinical operations activities, ensuring quality, timelines and budgets are met. Responsibilities include managing staff, providing clinical insights, updating stakeholders, tracking progress, driving vendor management, and implementing innovative operational solutions.

The Senior Manager will oversee the Global Development Quality Management System, focusing on quality event oversight, process improvement, stakeholder engagement, and governance activities. The role involves managing quality metrics, facilitating oversight meetings, and enhancing quality culture within the organization.

The Senior Manager of Business Operations Cost Management will oversee cost management for clinical trials, providing analytical support to development operations and finance teams. This role requires driving continuous improvement in business analytics, verifying cost estimates, and supporting strategic vendor relations. Key responsibilities include analyzing costs, modeling resource estimates, contributing to process improvements, and preparing analyses for decision-making meetings.

The role involves managing healthcare professional (HCP) engagement and contracting processes, ensuring compliance with regulations, and serving as a primary contact for commercial teams. Responsibilities include developing training materials, coordinating training programs, and collaborating with legal and compliance teams to implement best practices for efficiency.

The Manager, Global Procurement will develop and implement Global Clinical Category strategies, manage supply needs, collaborate with Clinical Operations, conduct negotiations, and leverage analytics to drive decision-making and cost efficiency within the biopharmaceutical industry.

The Senior Director Global Procurement oversees strategic sourcing and procurement for Regeneron's international operations, ensuring compliance with local market requirements while optimizing supplier engagement. The role involves leadership, project management, and partnership with senior leaders to facilitate global expansion and align corporate priorities with local needs.

The Associate Director, Global Procurement will lead procurement activities for the Clinical Drug Supply & Logistics category, manage supplier relationships, drive cost savings, and implement category strategies aligned with business needs. This role requires building influential relationships, running cross-functional teams, and having expertise in the biopharmaceutical market dynamics.