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Under the supervision of the President or designee, the Vice President - Academic Affairs / Chief Academic Officer (CAO) is responsible for providing vision, strategic direction, leadership and oversight of the academic programs, student support services and related activities and operations of the College.
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Work effectively with cross-functional partners including research and development, medical affairs, regulatory affairs, manufacturing, Health Economics Outcomes Research, Business Development & Licensing, market analytics, field sales organization, international and domestic operations, legal, scientific communications, professional education, training and development, health care compliance, etc.
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A career in Treasury Advisory, within Risk & Regulatory Advisory, will allow you to advise financial institutions on developing strategies to optimize financial performance and risk management across financial risks, including liquidity risk, market risk, counterparty credit risk and interest rate risk.
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Represent Regulatory CMC on cross-functional development/commercial teams and Regulatory Affairs teams. Participate in the development of the CMC regulatory strategy for small molecules, biologics and cell therapy submissions.
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The Director of External Affairs plays a pivotal role in advancing the mission of the Morris Museum through fundraising, special events, membership management, and community relations. The Angeletti Group invites nominations and applications to serve as the newly reimagined Director of External Affairs for the Morris Museum.
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Recruitment/Posting Title Patient Representative (Holocaust Survivors Program and Veterans Smile Program) Job Category Staff & Executive - Allied Health Department RSDM-Clinical affairs Overview.
$50,363 - $70,704Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Associate Principal Scientist will work closely with individuals from PaCES, Clinical Research, Regulatory Affairs, Biostatistics, Outcomes Research, and Operations to ensure COA endpoint strategies are consistent with and correctly executed to support the product strategy.
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Stay current with SailPoint product updates, industry trends, and regulatory changes to ensure the organization's IGA strategy remains effective and compliant. Implement and configure SailPoint Identity Governance and Administration solutions, ensuring alignment with organizational policies, regulatory requirements, and industry best practices.
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The Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the Senior Director, GMA Oncology ADC (Global Medical Affairs team lead for compound), is responsible for assisting with defining compound/program medical strategies and for leading select medical affairs projects within a specific compound or indication.
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The Director, Medical Research, is responsible for supporting strategic and operational activities of the Medical Affairs department and other functions at Intercept (e.g., R&D, Medical Safety) through real world evidence (RWE) generation.
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The Associate Director Global Medical Affairs Oncology (GMA), under the direction of the Senior Director, GMA Oncology (Global Medical Affairs team lead for compound), is responsible for assisting with defining compound/program medical strategies and for leading select medical affairs projects within a specific compound or indication.
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Recommend the employment of adjunct faculty to the Provost for Academic Affairs. Represent the Provost for Academic Affairs in serving as immediate administrative supervisor for all staff assigned to the Plainfield Campus Education Requirements Earned Doctorate Required Experience College teaching experience required, community college teaching preferred.
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It is paramount this individual has a deep understanding of Department of Veterans Affairs, Defense Health Agency, and Health and Human Services. In-depth understanding of the Department of Veterans Affairs, Defense Health Agency, and Health and Human Services.
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Collaborating with internal and external Customers and Service Providers, including but not limited to Clinical Research and Development, Global Study Management and Monitoring (GSMM), Project Management, Affiliates, Medical Affairs (MA), Regulatory, CMC, QA, Packaging Vendors, CRO’s, IRT Organizations, and Global Clinical Supply Chain Functional Operations to ensure all needs are met.
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Experience in process or analytical development, characterization, technology transfer, validation, / PPQ., facility fit, risk assessments, manufacture campaigns, process and plant modeling, regulatory filings (IND, BLA, PAS.
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regulatory affairs jobs Title: sr director Company: Thermo Fisher Scientific in Summit, NJ
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