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Provide regulatory guidance, general issue management and strategic stakeholder engagement support to Corporate Affairs and business leaders. Humana Director Public Policy, State Affairs Raleigh , North Carolina Apply Now Become a part of our caring community and help us put health first.
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Offering expert guidance from concept-through-commercialization, including product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled development costs, development risk mitigation, and accelerated market viability assessment.
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In this role you will lead global public affairs campaigns around key regulatory and public policy topics that impact the video game and entertainment industry. Lead strategy and execution of public affairs campaigns globally in partnership with the public policy team.
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The ideal candidate must possess strong accounting, compliance, regulatory reporting and operational expertise, an ability to communicate and work with various teams outside of Finance (such as Legal/Compliance, Trading Operations and other Product/Engineering groups), and a desire to make a significant impact on a dynamic, high-growth technology company.
$161,500 - $190,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Certifications (Preferred/a plus) : Certified Risk Manager (CRM), Certified Third Party Risk Professional (CTPRP), Certified Regulatory Vendor Program Manager (CRVPM), Lean Six Sigma Certification (i.e., Yellow Belt, Green Belt, Black Belt), or equivalent.
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System Office staff is responsible for executing the policies of the UNC Board of Governors and providing University-wide leadership in the areas of academic affairs, business and financial management, long-range planning, student affairs, research, legal affairs, and government relations.
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QATs are End-User Computing tools that support critical functions within Ally such as External Regulatory Reporting, Business Forecasting, Risk Appetite, Stress Testing, Pricing, Valuation, Capital, and Strategy.
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Work with project teams and plant personnel across our exterior building products manufacturing segments to ensure environmental compliance at new and existing facilities, including oversight and technical/regulatory support for air, wastewater, stormwater, hazardous waste, spill prevention and emergency response regulatory activities.
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The Campus Director of Academic Affairs is responsible for leading the delivery of quality student-centered, hands-on (active) learning. The Campus Director of Academic Affairs is responsible for maintaining high levels of academic quality and student satisfaction in order to retain and successfully graduate students, while operating in compliance with University policies and procedures as well as all state, federal and accrediting agency regulations.
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Help us shape the online experience of high-profile initiatives for our clients, including the National Football League and the U.S. Department of Veterans Affairs. The web content strategist will work full time as part of a team of user experience (UX), web design, development, and search engine optimization professionals.
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As a Clinical Scientist/Associate Medical Director, Clinical Development, this candidate will work cross-functionally to develop strong relationships with key stakeholders within Clinical Development, Clinical Operations, Regulatory Affairs, and Pharmacovigilance to support ongoing clinical trials and the lifecycle of the drug candidate.
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Provide medical support for the preparation of clinical protocols and protocol amendments as well as clinical sections of regulatory documents. Being a Clinical Scientist/Associate Medical Director, this person will also support the medical/clinical team with the interactions with Key Opinion Leaders (KOLs), principal investigators (PIs), and study sites.
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Support coordination and implementation of global HTA strategies, including dossier development and submissions, in collaboration with Medical & Scientific Affairs and Market Access colleagues.
$149,500 - $224,200 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
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Other divisions include Administration, Compliance & Accreditation, Comprehensive Health Services, Internal Affairs & Intelligence Operations, Post-Release Supervision & Parole Commission and Rehabilitation & Reentry.
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regulatory affairs jobs Title: sr regulatory affairs associate in Raleigh, NC
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