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Demonstrated 10+ years of professional experience in a government affairs, diplomatic, consulting, strategic advisory, or in-house capacity (e.g., government, business, NGO/not-for-profit, or law.
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You will partner with our Regulatory & Scientific Affairs team, and other cross-functionals, to stay current on/apply food laws and regulations affecting our company and products. You are the person who brings it all together with Nestlé requirements: Nutritional Requirement, Sustainability, external standards, and local regulatory framework.
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SOLV Energy seeks a Policy Associate with a passion for renewable energy and public affairs to join the Government Affairs team. The Policy Associate will support SOLV Energy by scheduling internal and external meetings, sending routine correspondence, maintaining various documents and databases, providing administrative support to the team, and by conducting policy research, such as tracking legislation, agency activities, and some regulatory processes.
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WHAT YOU’LL NEED TO SUCCEED (REQUIREMENTS): Bachelor’s degree in international affairs, economics, business, management, or related field. Advance the commercial partnership and support the Center’s advocacy efforts through member engagement, policy dialogues, regulatory submissions, educational reports, and strategic communications.
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2+ years of experience, preferably in a Congressional office, trade association, lobbying firm, advocacy organization, or other public affairs. Drafts routine correspondence, including e-mail communications to SOLV Energy team members, Capitol Hill, and regulatory agencies.
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Venn Strategies’ Critical Infrastructure practice group creates and implements government and public affairs strategies to meet our clients’ diverse needs, including cultivating meaningful relationships with Congress, the White House, and Federal Departments and Agencies, providing regulatory analysis, developing policy recommendations, facilitating stakeholder partnerships, and building coalitions that amplify client voices.
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HJF is seeking a Regulatory Affairs Coordinator to be responsible for assisting in the compliance of HJF research programs with applicable local, state and federal regulations for human subjects research, animal use research, recombinant DNA, and Health Insurance Portability and Accountability Act (HIPAA.
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Our teams include Communications, Community Impact and Investment, Community Finance, CRA Strategy and Program Management, the Government and Political Affairs Group, Regulatory Relations, and Strategy and Engagement.
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Our teams include Corporate Communications, Community Impact and Investment, Community Finance, CRA Strategy and Program Management, Government and Policy Affairs, Regulatory Relations, and EA Strategy and.
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Founded in 1871, this law firm has more than 200 lawyers practicing in areas such as antitrust, appellate litigation, biotechnology, construction, estate planning, governmental affairs, healthcare, intellectual property, and white-collar criminal defense.
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The Director must understand the entire preclinical and early clinical product development pipeline including product optimization, preclinical scale-up, and manufacture and toxicology, regulatory affairs, and early human clinical trials.
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Politically-minded (you’ll shape public opinion and influence the regulatory ecosystem) Policy monitoring: Staying abreast of policy developments to inform our teams, our clients and public affairs strategies.
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Experience with the following: Liaising with regulatory authorities, Training clinical trial site staff, Previous clinical trial work, Phase I or II experience, Regulatory compliance, Protocol development, Protocol navigation, Regulatory affairs, Clinical Research, IRB submissions, Clinical Trials, On-site visits, Data Integrity, Research, ICH/GCP, Strong writing skills with experience writing clinical research protocols.
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Our lawyers and legislative advisors serve domestic and international clients in all areas of corporate and business law, complex litigation, intellectual property, regulatory matters, and government affairs.
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G Regulatory Affairs ,Medical Writing) We are currently seeking an experienced and motivated individual to fill the role of Associate Director/Director Clinical Operations with our client, a small start-up immuno-oncology biotech company located in Montgomery County, Maryland.
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regulatory affairs associate jobs in Washington, DC
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