• Building Canva's enterprise reputation • Bringing customer success stories to life • Reaching key business audiences • Elevating executive thought leadership • Supporting enterprise launches and announcements

Role Description Join the growing team at LOCALiQ Direct, the Direct Mail channel of LOCALiQ. As a Direct Mail Subject Matter Expert (SME), you will help support prominent Regional and National brands with their Direct Mail initiatives. This position is focused on Project Management, helping to ensure that our clients’ campaigns are executed properly, on-time, and efficiently. Campaigns will be followed up with data and analytics to help inform strategies for the future. - The candidate must possess strong interpersonal skills and be an effective communicator (both verbal and written). - The Direct Mail SME will maintain regular contact with Sales Associates and Clients, but will not be cold-calling, prospecting, or given new sales quotas. - The candidate should be proficient with Microsoft Excel, PowerPoint, and Word. - This individual should be detail-oriented and possess the capacity to manage several projects at one time. - Advertising/Direct Mail sales or buying experience is preferred. Qualifications - Project Management Skillset - Advertising Sales Experience - Proficient in Microsoft Office (Excel, Word, PowerPoint) - Direct Mail Experience preferred - Ability to work through data, build strategies, etc. - Professional, Organized with attention to detail - Build trustworthy relationships with existing customers Requirements - The annualized base salary for this role will be $50,000.00 - $65,000.00. - Variable compensation is not reflected in these figures and based on the role, may be applicable. - Exact compensation may vary based on skills, experience, location, and union representation, if applicable. Company Description USA TODAY Co., Inc. is a diversified media company with expansive reach at the national and local level dedicated to empowering and enriching communities. We seek to inspire, inform, and connect audiences as a sustainable, growth-focused media and digital marketing solutions company. - Through our trusted brands, including the USA TODAY NETWORK, we provide essential journalism, local content, and digital experiences to audiences and businesses. - Our digital marketing solutions brand, LocaliQ, supports small and medium-sized businesses with innovative digital marketing products and solutions.

• Elevate Hart's market authority through high-quality thought leadership, blog content, press releases, and earned media. • Develop authoritative blog articles and long-form content on relevant topics for healthcare IT leaders. • Interview executives, subject matter experts, and clients to uncover insights and challenges. • Create content optimized for traditional SEO and answer engine optimization. • Write clear, credible content aligned with the needs of healthcare decision-makers. • Draft press releases for announcements, partnerships, and thought leadership campaigns. • Develop media materials like story briefs, company backgrounders, and award submissions. • Identify relevant media outlets and create targeted pitches for healthcare IT stories. • Recommend article topics and optimize content for executive search behavior.

Role Description The purpose of the Associate Director, Global Regulatory Affairs - Product Communications role is to provide leadership and influence to deliver accurate, balanced, and substantiated product and disease communications for assigned assets. The Associate Director partners with Regulatory Scientists, across Lilly brand teams, partner companies, and FDA Office of Prescription Drug Promotion (OPDP) to advise on regulatory requirements and expectations for compliant communications. Responsibilities - Review of Promotional Tactics and Communication - Serve as Regulatory representative for US brand teams, US Medical Affairs, and Corporate Business Communications for promotional tactics, internal field-based communications, medical affairs communications, and campaign tactics for media events - Provide high quality, prompt and conclusive regulatory advice that enables business partners to make well-informed decisions - Communicate regulator expectations by utilizing OPDP feedback received by Lilly, interpretation of applicable laws, regulations and guidances, and knowledge of FDA enforcement actions - Contribute to business risk mitigation strategies by following trends in external environment related to advertising, promotion and medical communication topics - Build, maintain, and utilize relationships with Lilly team members and partner companies, as appropriate, to effectively influence the implementation of appropriate communications - Initiate promotional tactic discontinuation plans for Regulatory-initiated events - Facilitate Interaction with FDA OPDP - Counsel internal partners on OPDP advisory strategy; collaborate with marketing and advertising agency in development of promotional proposals, and provide quality review of submission documents - Partner with US brand team to interpret OPDP advice and support any interactions with OPDP - Provide a well-timed and quality review of 2253 promotional material submissions to FDA - Collaborate with Other Regulatory colleagues - Engage US Regulatory Scientist in 1) development and analysis of promotional claims and suggest marketing on promotional strategy and 2) review of press materials and IR communications - Work closely with US Regulatory Scientist and Labeling Operations to lead labeling revisions to balance consideration of business implication and regulatory compliance - Communicate and share key information to enable seamless execution of US regulatory strategy and promotional activity - Lead/Influence/Partner - Engage in forums that share regulatory information across the organization, other Lilly teams, and business partners - Constructively challenge teams to reach the best solutions to issues - Create and lead in an environment that encourages open discussions on issues to achieve a robust outcome on business decisions Qualifications - Bachelor's Degree - 3+ years of industry-related experience in drug development and/or commercialization - Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1 Additional Skills/Preferences - Knowledge of FDA procedures and practices (CFR guidelines, Guidances, etc.) - Demonstrated ability to influence without authority and ability to deliver complex projects against a timeline - Strong communication skills (active listening, verbal, and written) - Demonstrated ability to apply systematic thinking/mindset to business problems and opportunities - Demonstrated effective teamwork skills; able to adapt to diverse interpersonal styles - Recent experience reviewing advertising and promotional materials for prescription drug products - Awareness of evolving regulatory reform initiatives and pending changes (Federal Register, media reports, etc.) Benefits - Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $132,000 - $193,600 - Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance) - Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities) - Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion