Drive scientific advancements as a Principal Medical Writer at ProPharma, focusing on high-profile pharmaceutical clients. This role emphasizes quality and efficiency in medical writing.

ProPharma, renowned for its expertise in regulatory and clinical services, is seeking a Principal Medical Writer with a robust background in clinical writing. With seven years of relevant experience, you'll author key documents, lead quality control efforts, and manage client relationships. Your contributions will help navigate the complexities of drug and device programs throughout their lifecycle.

Key Responsibilities:
• Create and edit essential clinical documentation
• Lead coordination of medical writing deliverables
• Mentor and support less experienced writers




• Ensure adherence to regulatory and quality standards
• Facilitate meetings and manage timelines effectively

Requirements:
• Bachelor's degree in a related discipline
• 7+ years’ experience in clinical writing
• Advanced understanding of regulatory submission processes
• Proficiency in document processing and project management
• Excellent collaboration and communication skills

Contribute your expertise to ProPharma and impact patient outcomes through your medical writing excellence.
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📌 Principal Medical Writer in UK/Ireland (Manitoba)
🏢 ProPharma Group
📍 Manitoba