💼 About This Role

You'll lead strategic integration of scientific information across publications, clinical transparency, and regulatory writing for a rare disease biopharma. Your core impact is ensuring seamless, compliant data flow from early development through lifecycle management. This role enables AI-driven modernization of scientific communication workflows.

🎯 What You'll Do

• Lead integration of clinical regulatory documents, trial transparency, publications, and library sciences
• Oversee lifecycle-based publication strategies aligned with regulatory and medical milestones
• Ensure strategic alignment of clinical trial disclosure and data sharing with global regulations
• Identify and implement AI-enabled tools to modernize scientific information workflows

📋 Requirements

• Advanced degree (PhD, PharmD, MD) preferred
• 12+ years in scientific publications, clinical transparency, or regulatory writing
• Exceptional collaboration skills to coordinate across multiple functions
• Experience with AI tools and process improvement in scientific communication

🎁 Benefits & Perks

• 🏖️ Remote work with occasional travel
• 🏥 Comprehensive health benefits
• 📈 Professional growth opportunities
• 💡 Impactful rare disease mission
• 🤝 Collaborative inclusive culture

📨 Hiring Process

Estimated timeline: 3-5 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 60 min
3. 3Panel Interview· 90 min