Jobs at Regeneron

The Canada Compliance Director leads compliance efforts across Canada, develops policies, coordinates with global teams, and mitigates compliance risks in the pharmaceutical industry.

The Office Manager coordinates daily office operations, managing vendors, supporting health and safety, and facilitating onboarding while enhancing workplace efficiency.

The Administrative Coordinator supports the Immunology team and General Manager by managing schedules, logistics, and administrative processes, ensuring efficiency across regions.

The Clinical Study Lead is accountable for the execution of clinical trials, overseeing study timelines, budgets, and compliance with SOPs and regulations. Responsibilities include leading study teams, managing vendors, developing protocols, ensuring data quality, and preparing for audits and inspections.

The Director Program Operations Leader manages clinical operations, overseeing quality, budgets, and timelines for oncology clinical trials, while ensuring compliance with regulations and SOPs.

The Senior Manager will lead AI integration into Global Development, focusing on developing scalable AI/ML solutions, enhancing data architecture, and collaborating across teams for effective AI implementation.

Manage Commercial Operations for Oncology Canada, collaborating with cross-functional teams to execute field operations, communications, and compliance processes efficiently.

The Program Operations Leader oversees complex clinical programs, ensuring quality, timelines, and budgets are met. They manage clinical operations, staff development, and vendor relationships, providing operational insights and driving strategic planning within clinical trial management.

The Associate Director oversees team management and external data processes, ensuring compliance with regulations and strategic execution in clinical data management.

Lead quality management in clinical trials, ensuring compliance, advising stakeholders, and driving quality initiatives within Global Development Quality systems.

The Clinical Study Associate Manager oversees clinical trial delivery, ensuring compliance with regulations and effective collaboration with vendors. Responsibilities include planning, risk assessment, monitoring data quality, and managing study-related tasks and reports.

The Associate Director leads External Clinical Data Management, ensuring compliance with best practices, coaching teams, and improving processes.

The Senior Manager AI Engineer will lead the development of AI solutions for Global Development, focusing on algorithms, data architecture, and stakeholder collaboration.