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The Innovation Protection Specialist is responsible for managing medical device development portfolios, focusing on innovation protection strategies, due diligence, and legal agreements. They collaborate with internal teams to support medical device R&D, provide metrics on intellectual property matters, and educate colleagues on compliance processes.

Responsible for delivering complex and strategic IT projects across Applications and Infrastructure for IOPS. Manage project delivery within budget, scope, quality, and time requirements. Communicate with team members and stakeholders to ensure project success. In-depth knowledge of Project Management, SDLC, PM Tools and Processes, Enterprise systems, and Life Sciences environment required.

The Manager Statistical Programming leads programming efforts for clinical study data, ensuring compliance with project standards. Responsibilities include development of analysis tables and managing programming for regulatory submissions. The role requires advanced expertise in SAS and experience with CDISC standards and complex data systems.

The Staff Accountant provides accounting analysis and reconciliation support for areas such as labor reporting, fixed assets, and intercompany activities at Regeneron. Responsibilities include assessing financial impacts, supporting inventory standard costs, collaborating with other departments, and applying GAAP for accounting tasks and reconciliations. Continuous improvement ideas and audit assistance are also part of the role.

The Associate Manager, Research Program Management will oversee the quality and accessibility of scientific project data, ensure data accuracy, manage discovery portfolios, and provide insights for decision-making. This role will also involve improving data management processes and mentoring others in the use of PPM systems and tools.

The Principal GMP Auditor is responsible for managing auditors' training, performing audits, ensuring compliance with GxP regulations, and collaborating with various stakeholders on quality management processes. Duties include maintaining audit documentation, overseeing auditor training programs, and leading supplier audits while ensuring adherence to regulatory standards.

The Sr. Manager Development Program Management leads operational direction for development programs in the drug development industry, managing multiple projects through their lifecycle and collaborating with cross-functional teams. Responsibilities include planning, budget oversight, risk mitigation, and facilitating communication across stakeholders to drive program success from preclinical to commercialization.