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Develop and implement global HEOR and RWE strategies for classical hematology products. Design and conduct HEOR, RWD, epidemiology, and COA studies; collaborate cross-functionally with Market Access, Medical Affairs, Clinical Development, and Commercial teams; support regulatory and reimbursement evidence needs; produce publications, regulatory submissions, and disseminate results to demonstrate product value and enable patient access.

The Associate Scientist will perform flow cytometry sorting experiments, maintain equipment, analyze data, and manage schedules while supporting research staff's objectives.

This role manages aggregate safety reporting activities, ensuring timely, compliant, and high-quality reporting throughout the product lifecycle.

The Senior Director Solutions Partner will align technology with research goals, manage cross-functional teams, and oversee informatics programs for therapeutic development.

The Control Room Supervisor oversees the Facilities Control Room team, ensuring effective alarm monitoring, employee performance management, and compliance with protocols. Responsibilities include documentation, team training, collaboration with stakeholders, and compliance investigations.

The role involves developing and implementing bioanalytical methods, collaborating with various teams, and contributing to the characterization of drug candidates in a fast-paced environment.

The Senior Associate Scientist will design and execute bioanalytical methods, support preclinical development, and collaborate with cross-functional teams, focusing on LC-MS and HPLC techniques.

The Associate Director of Enterprise Integration leads integration strategy, establishes governance, and oversees integration capabilities across the enterprise, focusing on architecture, API management, and continuous improvement.

The Director oversees customer data management, ensuring data integrity, governance, and collaboration across commercial systems. Responsibilities include leading data governance initiatives, managing MDM platform transitions, and mentoring data stewards.

The Associate Director provides legal counsel for Regeneron's manufacturing division, focusing on contracts, trade controls, and compliance with regulatory laws.