The Editor will perform quality control checks of clinical regulatory documents, ensuring they meet standards and guidelines, while training in advanced editing techniques.

Manage the engagement and contracting processes with healthcare professionals for Regeneron's Oncology portfolio, ensuring compliance and process improvements.

The HR Business Partner role supports 2000+ scientific employees in R&D, advising on organizational issues and collaborating with HR experts to meet business needs.

Provide administrative support to the Oncology Commercial team by coordinating logistics, managing funding requests, and handling travel arrangements.

Lead AAV production team, oversee research-grade AAV production, improve processes, mentor team members, and contribute to gene therapy development.

The Program Operations Leader oversees clinical operations in Clinical Trial Management, ensuring quality, timelines, and budgets while managing staff and collaborating with stakeholders.

The Senior Analyst is responsible for performance analytics in Global Procurement, focusing on reporting, metrics, e-sourcing event support, and data analysis from multiple sources.

The Senior Process Engineer provides technical support for manufacturing processes, assesses manufacturing requirements, and supports process transfers while ensuring compliance with safety standards.

The Senior Automation Engineer designs, implements, and optimizes automation systems in biopharmaceutical manufacturing, ensuring efficiency and compliance with regulations.

The Director, Patent Attorney will manage and protect intellectual property related to genetic medicines, advising on legal issues and coordinating patent filings. Strong collaboration with scientists is essential, along with handling administrative patent actions and supporting due diligence projects.

The Preclinical Program Manager oversees project plans in drug development, ensuring timelines and budgets are met while fostering cross-functional team collaboration.

The Manager of Financial Analysis prepares budgets, manages forecasts, and collaborates with teams to track expenditures and financial metrics for drug development.

The Sr. Administrative Coordinator supports senior leaders by managing calendars, coordinating meetings, onboarding, and maintaining records, while liaising with various departments.

The Associate Director, IT Quality leads quality operations, ensuring compliance with regulatory standards, developing validation strategies, and mentoring teams within IT and IS.

The Sr QC Technical Resource Specialist supports assay development and validation in QC, coordinates method performance, and communicates updates to partners. Responsibilities include performing analysis, driving improvements, and authoring technical documents.

The Executive Director leads strategic marketing initiatives for Dermatology, including team management, partnership alignment, and market analysis to drive brand success.

Oversee management of intellectual property in genetic medicines, protect therapeutics, support litigation, and manage patent portfolio and assessments.

The Staff Accountant will perform accounting duties, focusing on Product Revenue and SG&A expenses, ensuring compliance, accuracy, and timely reporting while collaborating with various departments.

Support the creation of visual reports, data integration and analysis, collaborate with sales teams, develop automated workflows, and improve data accessibility.

As a Global Procurement Intern, assist in strategic sourcing projects, data analysis, supplier selection, and collaborate with international teams on procurement functions.