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The Deputy General Counsel, Codman Specialty Surgical will report to the General Counsel, U.S. and will have primary responsibility for handling or managing a variety of general corporate and commercial contracting matters and will provide advisory services to CSS leaders, including the division president as well as sales, marketing, regulatory, quality, clinical and product development leaders.
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The Director, Drug Safety is responsible for planning, directing, coordinating and prioritizing activities of the product safety team and providing oversight of Pharmacovigilance (PV) vendors in all aspects of PV activities for products both marketed and in development.
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The CMO works closely with the Research and Development organizations driving overarching scientific leadership specifically in Hematology/Oncology, Bone Mineral, Rare Disease and Gene & Cell therapies, and in future therapeutic areas that may arise.
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The Senior Director, Ethics and Compliance, is a leader on our Ethics and Compliance team and a member of the US Leadership Team. Reporting to the Chief Ethics, Compliance & Privacy Officer, with strong partnership with senior leaders across Legal, Commercial, Medical, Clinical, Regulatory, Manufacturing, Development, IT, Finance and HR to build and integrate appropriate local compliance controls with our global compliance program.
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Understanding of philanthropy (mission, practice, trends) and fundraising practices (the development cycle, prospect and volunteer management policies and practices) The Senior Associate Director is a key member of the senior leadership team in Annual Giving managing and mentoring a number of Associate and/or Assistant Directors.
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Responsible for oversight of the outsourced analytical development activities associated with the development, validation, technology transfer, and line extension of drug product.
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Full cycle sales and pipeline building: prospect targeting, engagement, proposal development, negotiation, closing, and post-closing participation in ongoing account management and optimization activities.
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Responsible for supervising outsourced analytical development activities associated with the development, validation, and technology transfer for chemical regulatory starting materials, intermediates and active pharmaceutical ingredients.
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Experience with Medical Affairs activities including but not limited to, KOL engagement, clinical research, drug development, commercial planning and medical strategy. · Knowledge of drug launch activities, regulatory requirements governing clinical trials and experience in development strategy and the design of drug launch.
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Our curriculum focuses on the six ages and stages of early childhood development and engages children in hands-on learning activities that encourage them to explore and solve problems at their own rate of development.
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Demonstrating thought leadership through activities such as client presentations, webinars and client alerts, and/or participating in local, national and international scientific, professional and trade group meetings.
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Reporting to the Dean and Vice President of Academic Affairs, the Director of Assessment and Accreditation provides leadership and oversight of assessment activities for the purposes of program development and evaluation, accreditation, and institutional effectiveness.
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Reporting to the Vice President Global Medical Affairs, the Senior Director, Global Medical Affairs - LVV will provide overall strategic medical and scientific leadership for all Medical Affairs activities in the US & Europe in support of the development and commercialization of all Rocket lentiviral products which currently include investigational therapies for the treatment of leukocyte adhesion deficiency type I (LAD-I), Fanconi anemia and pyruvate kinase deficiency.
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Is a member of the CVP CKAD and Rare Disease Clinical Operations Leadership Team - including actively contributing to the leadership and future development of the area. Oversee and trouble-shoot clinical development program challenges, processes, activities and risk mitigation strategies pertaining to the conduct of clinical trials and key milestone deliverables, with direct reports/functional leads.
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Effectively summarize analyses or research outputs to clients and ZS teams, highlighting insights and presenting outcomes using Excel, PowerPoint, ZS's proprietary software, among others;Provide thought leadership and innovation within projects and practice areas;Participate in business development;Contribute to internal firm activities;Coach and mentor junior team members.
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leadership development activities jobs in Princeton, NJ
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