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As a Senior Director you will be responsible for leading HEOR-Epidemiology activities to inform, support, and strengthen global development and commercialization activities for our products in the oncology therapeutic area.
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Apply now to take your first steps toward living the Regeneron Way! Ability to work cross-functionally and present to internal partners, including senior management. Drawing on your expertise in epidemiologic study design and methods as well as on your knowledge of real-world data, you will design, conduct, and reporting of real-world evidence (RWE) studies.
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The Senior Medical Director, Immunology & Inflammation, will provide overall clinical scientific leadership for Regeneron's Immunology & Inflammation programs and have responsibility for our clinical development strategy and execution of clinical trials in this area.
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Reporting to the Global Patient Safety (GPS) Therapeutic Area (TA) Head, the Senior Director, serves as the first point of contact (POC) for all safety related issues for the compound(s) assigned within the therapeutic area (TA.
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As appropriate will also participate in business development activities and in collaborations with key partners outside of Regeneron. Additionally, Ph. D. degree or extensive laboratory research experience.
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In this role, a typical day might include:This Sr. Director position is directly responsible for all aspects of GPS activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.
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As a Senior Director in Pharmacometrics (PPK/PD, QP, or CP as appropriate), this individual will be responsible for managing PMx support for a number of programs in one or more therapeutic focus areas of the development portfolio.
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As a leader within the Global Clinical Trial Services (GCTS) group, the Senior Director will engage and work closely with other cross functional partners and senior leaders within Development Operations and Portfolio Planning (clinical study teams, senior level management, and external vendors) to align and implement a portfolio-wide Study start-up strategy.
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