Senior Content Copywriter

📋 Description

• • Lead the creation of long-form content including blogs, thought leadership pieces, case studies, and research-driven articles that communicate complex clinical, regulatory, and drug development topics to patients, healthcare professionals, and BioPharma partners.
• • Adapt core messaging into tailored copy across multiple channels—website, email campaigns, social media, and promotional materials—ensuring tone, clarity, and audience relevance are optimized for each platform.
• • Translate highly technical information about clinical trials, Expanded Access Programs, and Real-World Data collection into accessible, accurate, and responsible language without diluting scientific integrity or regulatory nuance.
• • Maintain strict editorial discipline in a regulated health-tech environment, applying rigorous fact-checking, claims sensitivity, and compliance-aware writing to ensure all content meets legal, ethical, and industry standards.
• • Collaborate closely with internal subject matter experts—including clinical, regulatory, and scientific teams—to convert incomplete, technical, or fragmented inputs into polished, review-ready drafts that align with brand voice and strategic objectives.
• • Utilize AI tools responsibly to enhance drafting efficiency, content repurposing, and research speed, while preserving originality, factual accuracy, and human editorial oversight in all outputs.
• • Drive consistency in editorial standards across all published materials, ensuring content feels distinctly myTomorrows in tone and quality, reducing revision cycles and accelerating approval timelines.
• • Improve organic social media performance by crafting platform-specific, engagement-optimized copy informed by audience insights and performance metrics, adapting strategy over time to increase reach and impact.
• • Build and maintain a reliable pipeline of high-priority content that supports key business initiatives, including patient recruitment, partner communications, and market expansion efforts.
• • Ensure all content reflects a deep understanding of the global drug development ecosystem, including the roles of patient advocacy groups, trial sites, and BioPharma companies, and aligns with myTomorrows’ mission of accelerating treatment access.
• • Contribute to brand credibility by producing content that builds trust with diverse stakeholders—patients seeking hope, HCPs navigating complex options, and BioPharma partners requiring precise messaging.
• • Continuously refine content strategy through feedback loops with marketing, product, and compliance teams, ensuring alignment with evolving regulatory landscapes and company goals.
• • Act as a content authority within the organization, mentoring junior writers and setting benchmarks for quality, clarity, and compliance in all written outputs.
• • Support global initiatives by creating content that resonates across cultures and regions, while maintaining strict adherence to US regulatory and communication standards in a remote, international environment.