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Continues to develop and nurture long-term strategic partnerships with clinical specialists, societies, collaborative groups, advocacy groups, and other external partners representing Regeneron.
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Responds to customer inquiries with integrity, compliance, and adherence to legal, regulatory, and Regeneron guidelines, policies & procedures, to support the accurate use of products and services.
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Regeneron is currently looking for a Senior Device Development Engineer to join our Process Sciences Drug Product Engineering department. Apply now to take your first steps toward living the Regeneron Way.
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To be considered you are required to have 8+ years of relevant experience, which includes 4+ years working as a Medical Science Liaison within the Oncology/ Hematology field or a combination of experience working within Oncology/ Hematology (lymphoma and/or multiple myeloma is preferred.
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We are looking for an Associate Director, within our Clinical Pharmacology group.
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This is to ensure the distribution of clinical and scientific information regarding in-development or commercialized Regeneron products in a timely, ethical and customer-focused manner. Identifies and brings impactful information & insights that improve the value and appropriate use of Regeneron products back to internal partners.
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Director Statistical Programming provides leadership and support to the teams on all statistical programming matters according to the project strategies within therapeutic area(s). Meets with Statistical Programming management team routinely to evaluate and develop solutions for project resourcing, quality, timelines, budget, standard processes, and training needs.
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This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.
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Working in matrix environment including cross-functional commercial partners, within a pharmaceutical corporate environmentPreferred experiences include:Established relationships with KOLs in malignant hematology and knowledge of institutions focused on Hematologic MalignanciesDrug launch experience is strongly preferred#msl #medicalscienceliaison #hematologyDoes this sound like you.
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As an Associate Director, Field Medical Affairs you be a field facing representative engaging in the exchange of scientific data, medical or information with KOLs, HCPs, researchers, pharmacists and population-based decision makers.
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Sustains expertise in product/ molecule data, disease state management, emerging therapies, and the competitive landscapeResponds to customer inquiries with integrity, compliance, and adherence to legal, regulatory, and Regeneron guidelines, policies & procedures, to support the accurate use of products and servicesSupports clinical research activities through phases 1-4, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ specialists and sites.
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Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Establishing, fostering, cultivating and maintaining peer relationships with KOLs in Hematological MalignanciesAct as the primary clinical/scientific resource to HCPs in the territory for information pertaining to disease state and Regenerons product ensuring awareness and understanding.
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To be considered for this position, at a minimum, you need a Clinical/Science degree (MD, OD, PharmD, PhD, DVM) with strong preference for candidates with 3 + years of field medical affairs experience in Ophthalmology.
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Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence. Establishing scientific relationship with investigators and internal Medical Affairs, supports investigator-initiated study (IIS) concept program.
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To be considered for this position at a minimum you need a Clinical/Science degree (MD, PharmD, PhD, DVM with 5 + years related work experience (clinical, managed care, or industry experience) in Ophthalmology is preferred.
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Company: Regeneron
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