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Advanced life science degree or certification in Regulatory Affairs Sciences preferred. In this role, a typical day might include:The Regulatory Intelligence Manager performs proactive global monitoring and surveillance of changes in the regulatory landscape focused on the drug development lifecycle, i.e., preclinical through commercialization, as well as disseminate relevant regulatory intelligence information to Regeneron stakeholders.
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To be considered for the Associate Biotech Production Specialist role you must be able and willing to work a 2nd or 3rd with weekend shift, you must have one of the following; BS/BA in Life Sciences or related field or AS/AAS Degree/Certificate in Biotechnology/Biological Science, or an equivalent combination of education and experience.
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Resolves novel problems requiring creative application of advanced skill, training, and educationMay serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriateTo be considered for this role, you must have a Bachelor’s Degree, Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) is preferred.
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Bachelor's degree in business, finance, science/technology, or related field and 12+ years of pharmaceutical/biotech industry experience and a minimum of three years in program, portfolio and/or alliance management (or equivalent management consulting experience.
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To be considered for this role, you must have a Bachelor’s Degree Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). Apply now to take your first step towards living the Regeneron Way.
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We are looking for a Lead LIMS Developer who will support our new Regeneron Cell Medicines (RCM) unit, located in the heart of Cambridge, MA. RCM is dedicated to novel cell therapies, translating science to medicine for our patients.
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To be considered for this position, you must have a Clinical/Science Degree required (e.g., MD, PharmD, PhD) with a minimum of 5 years related work experience (clinical, managed care, or industry experience.
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We provide clinical and health economic information that enhances the value and appropriate use of Regeneron products. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
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Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions.
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Regeneron is seeking a Manager to join the Regulatory Intelligence Group! Experience and solid knowledge of Pharmacovigilance specificallyProficiency in one or more of these additional areas is a plus: CMC/Mfg., Clinical development and trial execution, Regulatory, Real-World Data and Real-World Evidence, Cell and Gene Therapy, Medical Device, IVD/CDxExperienced in understanding and interpreting regulatory guidelines and documents.
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Description As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within Respiratory. Experience in Immunology is required; Respiratory is preferred, as is experience as a field medical representative.
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G MD/DO/MBBS, PhD, PharmD) and 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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