Elevate your career as a Lead Medical Writer with ICON, where integrity and collaboration are paramount. Oversee high-quality regulatory documents that drive recent medicines to patients faster. As a Principal Medical Writer, you will manage medical writing workstreams while ensuring adherence to timelines and quality standards.

This role requires expertise in preparing clinical study reports and protocols, while collaborating with clinical research, biostatistics, and regulatory teams. Mentoring junior writers and staying updated on regulatory trends will also be crucial in your responsibilities. Key Responsibilities:

- Prepare and review clinical study reports accurately
- Collaborate with cross-functional teams for effective document development




- Provide guidance on best medical writing practices
- Mentor junior medical writers to build expertise
- Act as lead writer for complex regulatory submissions Requirements:
- Bachelor’s degree in life sciences or related field
- Significant medical writing experience in regulatory submissions
- Strong understanding of industry standards
- Exceptional writing and editing skills
- Excellent communication and collaboration abilities Bring your medical writing expertise to ICON and influence the future of patient care.

📌 Lead Medical Writer at ICON (Montreal)
🏢 ICON Strategic Solutions
📍 Montreal