Shape the future of medicine as a Principal Medical Writer with ProPharma. This role centralizes around creating regulatory documentation and leading medical writing projects.

ProPharma seeks an experienced medical writer with a proven track record in clinical research documentation. You will lead the writing of complex regulatory submissions and provide mentorship to junior team members. Collaboration across multiple departments is key for producing high-quality deliverables that meet strict timelines.

Key Responsibilities:
• Produce and oversee clinical and regulatory documents
• Interact directly with clients and reviews
• Mentor less experienced writers and conduct training sessions
• Manage project timelines and deliverable schedules
• Implement QC reviews for documentation accuracy

Requirements:
• Bachelor’s degree in a medical or scientific discipline
• At least 7 years' experience in medical writing
• Robust understanding of regulatory requirements
• High proficiency in MS Word
• Exceptional organizational and communication skills

Utilize your expertise to contribute to ProPharma's commitment to improving patient health through quality documentation.
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📌 ProPharma Principal Medical Writer Role (Ontario)
🏢 ProPharma
📍 Ontario