💼 About This Role

You'll lead development of high-quality medical and regulatory documents in a global life sciences environment, supporting clinical research and drug development. Your core impact involves translating complex scientific information into clear, compliant documentation while collaborating with cross-functional teams. This role offers the chance to contribute to innovative therapies and mentor junior writers.

🎯 What You'll Do

• Lead preparation and delivery of regulatory writing documents
• Develop clinical study protocols, reports, and investigator brochures
• Coordinate document review cycles and stakeholder feedback
• Mentor junior medical writers on complex projects

📋 Requirements

• 3-5 years of medical writing experience in biopharma or CRO
• Experience writing clinical and regulatory documentation
• Understanding of FDA and ICH guidelines

✨ Nice to Have

• Experience mentoring junior team members
• Advanced degree in life sciences

🎁 Benefits & Perks

• 🏠 Flexible remote work
• 🌍 Exposure to diverse therapeutic areas
• 📈 Career development programs and training
• 🤝 Collaborative and inclusive culture
• 💰 Competitive compensation and rewards

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical/Writing Assessment· 60 min