Become a key part of our client’s medical affairs team as a Senior Medical Writer in Kimberley. Leverage your writing expertise and pharmaceutical knowledge to create vital regulatory and educational documents.

This role demands a proven Medical Writer with a minimum of five years’ experience in the pharmaceutical or biotechnology sectors. You'll craft documents for diverse audiences, ensuring scientific accuracy and adherence to guidelines such as ICH and FDA. Managing multiple projects while mentoring junior writers is a critical component of this impactful position.

Key Responsibilities:
• Write and review clinical study reports and regulatory documents
• Ensure compliance with ICH, FDA, and EMA guidelines
• Collaborate with R&D;, regulatory affairs, and marketing teams




• Oversee document timelines and project budgets
• Mentor junior writers and contribute to style guides

Requirements:
• Bachelor's degree in life sciences; advanced degree preferred
• At least 5 years of Medical Writing experience
• Solid knowledge of clinical trial and regulatory processes
• Excellent organizational and communication skills
• Proficiency in Microsoft Office and document management systems

Drive communication of medical data and support impactful submissions as a Senior Medical Writer.
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📌 Senior Medical Writer in Kimberley (British Columbia)
🏢 Placements24
📍 British Columbia