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They will be responsible for coordinating submissions to local regulatory bodies including the Institutional Review Board (IRB) under the supervision of the Regulatory Affairs Manager.
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The Title IX Coordinator reports to the Dean of Student Life and has the primary responsibility of coordinating and implementing the University’s compliance efforts with Title IX, working closely with the Vice President of Student Affairs, Associate Vice President of Human Resources, Director of Equal Opportunity, General Counsel, and other administrative leaders, and has no other duties that create a conflict of interest.
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Participate in the administrator on-call weekly rotation with the Associate Vice President for Student Affairs, Director of Residence Life, and other administrators. Serve as a member of the Housing Accommodations Committee, Student Affairs Committee on Diversity, the Admissions Program Advisory Committee, and others as determined by the Director.
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Complies with all regulatory guidelines outlined in Cadet Command Regulation 14-2, JROTC Program Organization, Administration, Operation, Training and Support and Cadet Command Regulation 145-8-3, Organizational Inspection Program.
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Director, CMC Regulatory Affairs. 15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
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In coordination with the Division VP of Marketing and Corporate Affairs, documents a crisis communication strategy for the Division in line with crisis communications best practices and in alignment with the Corporate crisis communication plan/policies.
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Communications / Contacts Internal - Departmental staff, business unit leaders/representatives, accounting managers, treasury and finance personnel, regulatory affairs cost of service department staff; and BHE corporate consolidations External - Federal Energy Regulatory Commission (FERC), Corporate Noteholders, Kansas Dept of Health & Environment, Environmental Protection Agency, auditing firms, IRS, pipeline journals.
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Providing expert counsel and collaborating with our Government Affairs staff and corporate subject matter experts on key strategic and high profile issues, projects, initiatives, and programs.
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The Associate Director, Immunology Medical Affairs Data Analytics will collaborate with colleagues across the Immunology US Medical Affairs organization, such as Medical Heads, MSL Field Directors, Integrated Evidence Team Leads, as well as data analysts in the business units with whom Medical Affairs collaborates: Commercial (Franchise and Brand), Global Medical Affairs, Janssen Scientific Affairs, and Strategy Analytics and Transformation.
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Johnson and Johnson Inc. is hiring an Associate Director, Immunology Medical Affairs Data Analytics. The Associate Director, Immunology Medical Affairs Data Analytics role is responsible for generating, integrating and translating insights to support Medical Affairs strategy and to drive organizational action for US Medical Affairs.
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As a direct report to the Provost and Vice President for Academic Affairs, the Associate Vice President of Research and Sponsored Programs (AVP RSP) leads and manages the Office of Research and Sponsored Programs.
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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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Organization Janssen Scientific Affairs, LLC (6120) The Immunology Medical Affairs Data Analytics role is accountable to lead disease-area specific data projects in support of Medical Affairs Strategy.
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2 years of Medical Affairs experience. Job Function Medical Affairs. Market research, business intelligence, business analytics, strategic planning, or management consulting preferred. Diversity of experience is preferred, with proven learning agility to support the growing Immunology portfolio.
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Deliver innovative solutions to evolve our field business model (KOL identification platforms, JET solutions, iConnect enhancements, etc) Remote work options in the United States may be considered on a case-by-case basis and if approved by the Company.
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regulatory affairs jobs Title: sr director Company: Planet Pharma
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