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The DCAMM Director of External Affairs reports to the Chief of Staff and serves as an important member of the Executive Office team, helping DCAMM contribute to the Administration’s policy and goals related to decarbonization and housing, as well as access and opportunity for underrepresented populations, in addition to supporting the core mission of the agency in real estate, planning, design and construction.
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The position requires a history of experience in gene therapy, preferably within the rare disease space, and will be responsible for managing and communicating with external regulatory consultants as needed.
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As lead of the Study Core Team the CS will lead via a matrix organization Epidemiology, Biostats, Clinical Operations, Medical/Scientific Affairs, Regional, Pfizer laboratory assay group, and external team members.
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This individual may serve as a liaison to external contract safety providers and company personnel for safety issues, working in close collaboration with colleagues from Clinical Operations, Regulatory Affairs, Quality and Medical Affairs.
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This opportunity will offer you the chance to grow your Regulatory Affairs CMC expertise across a range of disciplines such as nucleic acid therapeutics, lipid-nanoparticle drug delivery, viral delivery systems, and a range of cell therapy products.
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This is a senior role, working closely with the Portfolio Manager, External Investment Management - Public Markets, Senior PM's, Chief Investment Officer (CIO), and other senior Investments leaders and staff, across asset classes, with a primary focus on public equities investments with our external investment management partners.
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Position SummaryThis position is a key leadership role for the development of the In Vivo franchise at CRISPR. Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross-functional teams and partners to bring multiple novel therapies to patients.
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Collaborate: Integrate protein engineering and cutting edge efforts efficiently into product offerings and engage with external collaborators in discovery of biologics. At ADS, we employ cutting-edge technologies in molecular biology, protein sciences, B-cell cloning, phage and yeast display, novel antibody formats and analytics to identify and optimize antibody-based therapeutics.
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As a pivotal member of the rare disease team, the Global Marketing & Commercial Lead for Rare Disease will report to the General Manager and drive the execution of a robust commercial strategy for our portfolio, initially focusing on PA and MMA. This strategic role requires collaboration with multidisciplinary teams across R&D, Medical Affairs, Value and Access, and Supply Chain to ensure cohesive efforts within Moderna.
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Responsible for aspects of external collaborations from management of joint project teams and scientific decisions to ensure achieving stage gates and milestone criteria on timely manner and within allocated budgets.
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In this central role, the Associate Director will engage with multiple internal and external stakeholders such as Medical Affairs, Clinical Development, Translational Research, Clinical Pharmacology/DMPK, HEOR, Biostatistics, external authors, investigators, publishers, and medical communications agencies.
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Our mission is to facilitate long-term stable communication between external world and the patient’s brain, with ultrasoft materials that minimize the immune response, minimal invasiveness implantation technique, ultra-high bandwidth that allows minimal latency and enhanced accuracy.
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Previous experience or exposure to regulatory, government, or external affairs. And our Water Quality companies—Aquatic Informatics, ChemTreat, Hach, McCrometer, OTT HydroMet, Sea-Bird Scientific, Trojan Technologies, and XOS—help customers manage, treat, purify, and protect the global water supply, from municipal and wastewater treatment facilities to lakes, rivers, watersheds, and oceans.
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Comprising Communications, Government and Regulatory Affairs, Labor and Workforce, and Community Engagement, the External Affairs Department is responsible for shaping government policy to support offshore wind development and building support for projects by engaging with key stakeholders and delivering local benefits.
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The Senior Director of Regulatory Affairs Chemistry, Manufacturing, and Controls (RCMC) will provide strategic as well as operational leadership of global CMC activities related to Cell & Gene Therapy (GCT) leading to successful registration and life-cycle management of unique and technologically complex products.
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edge external affairs jobs Company: Capital One in Boston, MA
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