Company: Regeneron Pharmaceuticals, Inc
The Associate Director, Senior Medical Advisor assists in the development of medical strategy, planning, and execution of oncology-related medical affairs activities at Regeneron UK. This hire provides scientific and/or medical expertise by thoroughly understanding oncology, particularly immuno-oncology, and serves as a scientific/medical resource. The Associate Director will work in a multifunctional, matrix organization, closely with [...]Read More... from Associate Director, Medical Advisor (Oncology) See details
The Associate Director, Senior Medical Advisor assists in the development of medical strategy, planning, and execution of oncology-related medical affairs activities at Regeneron UK. This hire provides scientific and/or medical expertise by thoroughly understanding oncology, particularly immuno-oncology, and serves as a scientific/medical resource. The Associate Director will work in a multifunctional, matrix organization, closely collaborating [...]Read More... from Associate Director, Medical Advisor (Oncology) See details
Job Description: The Director/Sr. Director EHS & Security will oversee all Health, Safety, Environmental and Security operations to ensure compliance with or exceed local and national environmental regulatory requirements for the IOPS division of Regeneron in Limerick. Key Responsibilities: Drive a strong safety culture, programs, and behavioral awareness. Develop and implement EHS and Security policies, [...]Read More... from Director/Senior Director EHS See details
Global Procurement Intern We are seeking a dedicated and enthusiastic Global Procurement Intern to join our international team at Regeneron. This role offers a unique opportunity to support the global expansion of procurement across various strategic projects. As a Global Procurement Intern, you will play a crucial role in developing and deploying strategic sourcing initiatives, [...]Read More... from Intern, Global Procurement: International Markets See details
At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. As Key Account Manager, you will play a [...]Read More... from Key Account Manager – East of England, East Anglia and Essex See details
At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. As Key Account Manager, you will play a [...]Read More... from Key Account Manager – Southwest and South Wales See details
At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. As Key Account Manager, you will play a [...]Read More... from Key Account Manager – Scotland, Northern Ireland and Northeast England See details
The Manager Clinical Study Lead (CSL) may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. The CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron [...]Read More... from Manager Clinical Study Lead See details
The Senior Clinical Study Lead (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance [...]Read More... from Senior Manager, Clinical Study Lead See details
The Principal Statistical Programmer will lead and support all programming activities per the project strategies and should be able to work independently implementing and driving the programming to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, collaborators, and [...]Read More... from Principal Statistical Programmer See details
