💼 About This Role

You'll lead global medical writing strategy for early-phase clinical development in a highly innovative pharmaceutical environment. You'll oversee creation of regulatory-compliant documents and build a high-performing, forward-thinking team while driving digital transformation and AI integration.

🎯 What You'll Do

• Lead development of global medical writing strategy for early clinical development
• Oversee creation of high-quality regulatory and clinical documents
• Manage capacity planning, resource allocation, and vendor partnerships
• Champion process improvements, digital transformation, and AI adoption

📋 Requirements

• Advanced degree (MS or PhD) in Life Sciences or related field
• 10+ years experience in medical writing within pharma, biotech, or CRO
• 5+ years leadership experience managing high-performing teams
• Strong understanding of clinical drug development and regulatory documentation

✨ Nice to Have

• Experience with AI-driven clinical development initiatives
• Experience in early-phase clinical development
• Familiarity with digital transformation in regulatory environments

🎁 Benefits & Perks

• 💰 Competitive base salary $200k-$316k
• 🏥 Comprehensive health, dental, vision insurance
• 🏖️ Paid time off and flexible work-life balance
• 📈 Retirement savings plan with employer contributions
• 📚 Learning and leadership development programs

📨 Hiring Process

Estimated timeline: 4-6 weeks · AI estimate

1. 1Recruiter screen· 30-45 min
2. 2Hiring manager interview· 60 min
3. 3Leadership panel interview· 90 min