Job Description

Step into a pivotal role as a Principal Medical Writer, focusing on high-quality documentation and collaboration across clinical research projects. This position values expertise in both writing and regulatory compliance.
As a Principal Medical Writer, you will oversee the creation of essential clinical documents and lead project teams. You will ensure that all written materials meet strict regulatory standards while mentoring new talent in the field. Your proactive approach and extensive experience will directly impact the quality of our deliverables.
Key Responsibilities:
• Manage clinical documentation and regulatory submissions
• Lead team meetings and oversee project timelines
• Author and edit various complex documents
• Train and mentor junior medical writers
• Perform peer reviews of writing contributions
Requirements:
• Bachelor’s degree or higher in a related field
• Minimum of 7 years in clinical/regulatory writing
• Comprehensive understandi...

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