• Own and evolve the brand positioning across channels, grounded in business priorities, audience insight, and market differentiation. • Develop messaging frameworks, narrative pillars, and communication strategies that strengthen and reinforce brand positioning. • Lead brand storytelling initiatives across campaigns, product marketing, PR, web experiences, and lifecycle communications. • Write and edit high-impact brand messaging and copy that delivers clarity, consistency, and emotional resonance across all touchpoints. • Collaborate closely with the Creative Director to shape brand concepts, narratives, tone of voice, and strategic messaging. • Partner with SEO and Growth teams to create messaging that balances brand identity, audience relevance, and performance objectives. • Translate audience insights, keyword research, and growth priorities into compelling, human-centered brand narratives. • Ensure consistency in brand voice, positioning, and messaging across all customer-facing experiences. • Operate as a senior brand voice across Growth, Product Marketing, Design, and cross-functional stakeholders. • Serve as a strategic thought partner by influencing messaging direction, positioning decisions, and communication strategy. • Evaluate messaging and campaign performance, test positioning hypotheses, and refine strategies based on insights and experimentation. • Build scalable systems, workflows, and editorial processes that support sustainable brand growth and operational efficiency. • Provide strategic direction and feedback to freelancers and agencies while maintaining high creative and editorial standards. • Leverage tools, templates, and AI-assisted workflows to improve efficiency, ideation, and quality at scale.

• Join Us as a Safety Writer III– Make an Impact at the Forefront of Innovation • You will be responsible for the planning, coordination, and delivery of safety writing services for clinical trial and/or marketed product projects • Perform day-to-day safety writing and related activities within a highly regulated pharmacovigilance environment • Conduct data review, authoring, quality review, and senior review tasks on, and project manages a wide range of clinical trial and marketed product safety writing deliverables • Functions in a lead role, serving as the primary point of contact for assigned safety writing deliverables • Ensures that assigned safety writing and project management tasks are conducted in accordance with company policies and procedures, contractual agreements and applicable regulations • Participates in departmental initiatives • Performs routine project implementation and coordination activities for assigned safety writing projects

• Conducts data review, authoring, quality review, and senior review tasks on, and project manages a wide range of clinical trial and marketed product safety writing deliverables. • Serves as a consultant on higher complexity deliverables. • May additionally provide support for scientific safety services on an ad-hoc basis. • Uses multiple PPD and client systems. Interacts with PPD/Evidera project team members and clients. • Functions in a lead role, serving as the primary point of contact for assigned safety writing deliverables. • Exercises independent judgment to troubleshoot and resolve project issues and to identify areas for improvement. • Serves as primary point of contact in absence of the manager. • Supports management with delegated oversight of team training/mentoring. • Ensures that assigned safety writing and project management tasks are conducted in accordance with company policies and procedures, contractual agreements and applicable regulations. • Reviews regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices and procedures. • Participates in/leads departmental initiatives; Serves as a subject matter expert in designated area. • Performs routine project implementation and coordination activities for assigned safety writing projects (including functional service provider clients), including leading kick-off meetings, managing communications and data requests, participating in client meetings, audits and inspections, and reviewing of metrics and budgets.

• Manage the delivery of global aggregate safety reports, risk management plans (RMPs), regulatory authority assessment report responses, and custom safety reports, for both developmental and marketed products. • Ensure that the team is provided with sufficient resources to deliver services in accordance with company policies and procedures, contractual agreements and applicable regulations. • Maintain good communication with other functional groups concerning safety writing activities. • Prepare for and present proposals and bids on behalf of the Safety Writing Team. • Prepare for and contribute to client and internal meetings, audits and regulatory authority inspections. • Participate in departmental initiatives and task forces for process improvement and overall department management. • Review regulatory/pharmacovigilance publications and information sources to keep updated on current regulations and practices. • Provide input on PV procedural documents. • Participate in meetings to communicate quality, budgetary or operational information in relation to safety writing services. • Manage staff of experienced professionals, which may include interviewing and selection, job description preparation, professional development, goal setting, performance management, coaching and mentoring, employee counseling, and separations. Approve courses of action on salary administration, hiring, corrective action, and terminations. Review and approve time records, expense reports, requests for leave, and overtime.