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The Cardiovascular & Metabolism Regional Medical Scientific Director is a credentialed (i.e., PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in bidirectional exchange of scientific or medical information with Scientific Leaders (SLs.
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Education : MD, PhD, PharmD or other relevant advanced degree required. Our Medical Affairs function serves as a valued strategic partner with Clinical, Commercial, Regulatory, and Market Access on therapeutic solutions to support patients' needs.
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We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio.
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The Senior Medical Science Liaison is a remote, field-based, external customer-facing member of the US therapeutic area medical unit team, responsible for analyzing, interpreting and disseminating scientific data, acquiring and translating customer insights, fostering external expert networks, and compliantly connecting customers to Takeda in order to advance medical strategy and improve patient outcomes.
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Graduate of an accredited school of pharmacy with BS Pharm or PharmD Degree. Prepares medications by reviewing and interpreting physician orders; detecting therapeutic incompatibilities.
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Scientific degree; advanced degree (e.g., MS, PhD, MD/DO, PharmD, NP, MSN) preferred. Substantial understanding of relevant therapeutic area required. This individual will be responsible for interacting at Director and VP levels within Medical Affairs & HEOR functions and other internal stakeholders (e.g., Corporate Analytics and Operations (CA&O), Commercial, Office of Ethics and Compliance (OEC), Legal, etc.
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Advanced degree in a scientific discipline: MD, PhD, PharmD. Provide inspirational leadership to the US Medical Affairs Immunology (Non-Alliance) team (Medical Directors, Medical Science Liaison Managers, MSLs) by cultivating a culture of teamwork and collaboration to ensure the delivery of key priorities, while attracting, developing and retaining top talent.
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Doctorate degree (PharmD, MD, DO or PhD); will consider NP/PA with clinical experience in relevant therapeutic area. Collecting, analyzing, and communicating information concerning therapeutic area, treatment options, emerging standards of care, and competitive intelligence.
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G M.D., PhD, PharmD, DPH, EdD) or an advanced degree in Pharmacology, Pharmacy, Medicine, Nursing or equivalent experience is preferred;Working knowledge of FDA, OIG requirements;A minimum of 1 year MSL experience or 2 years experience working within the pharmaceutical/biotech industry or post-graduate fellowship experience in a hospital or industry setting.
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Demonstrate advanced knowledge regarding Takeda disease areas and products as well as therapeutic area competitor landscape; analyze and interpret complex scientific information and disseminate to KOLs/HCPs in a compliant, fair-balanced, and non-misleading manner.
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Maintain business and clinical knowledge of the Rare Disease Diseases treatment landscape including current treatment strategies, current and pending competitors, and new therapeutic developments.
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Advanced degree in Life Sciences, Business operations, or related field: an MBA with 8 years of relevant medical experience, PhD/PharmD with 6 years of experience, or an MD with 3 years of experience.
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The candidate should have an M.D. with board certification/eligibility in hematology/oncology,or a Phd,PharmD with at least 5 years of drug development experience. Provide initial clinical designs for future trials including partnering with research, translational oncology, biostatistics, clinical operations, regulatory and pharmacology for input/alignment and presentation at the Therapeutic Development Team meetings.
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The MSL must demonstrate deep therapeutic expertise, understand territory and market influences, engage scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic and tactical plan – while functioning within the Novartis Code of Conduct, Ethics/Compliance policies and Working Practice documents.
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MS/PharmD/PhD in Chemistry, Biology, Biochemistry, business, or related healthcare area. Working knowledge of relevant therapeutic areas and experience working within development of preclinical through translational stage clinical studies.
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