Remote | United States | Project-Based Independent Contractor Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements Help Shape the Future of AI in Pharmaceutical What if your expertise in regulatory writing, CMC documentation, and global pharmaceutical submissions could help art
About the role
Remote | United States | Project-Based Independent Contractor
Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements
Help Shape the Future of AI in Pharmaceutical
What if your expertise in regulatory writing, CMC documentation, and global pharmaceutical submissions could help artificial intelligence better understand regulatory requirements, technical documentation standards, and submission best practices?
At Volga Partners , we're connecting experienced pharmaceutical professionals with opportunities to contribute to the development and evaluation of advanced AI models.
We're seeking experienced Regulatory CMC Submission Writers who can apply their regulatory writing expertise, scientific knowledge, and technical documentation experience to evaluate AI-generated pharmaceutical and regulatory content.
This isn't a traditional regulatory writing position. You won't be authoring submissions for health authorities, coordinating submission timelines, or supporting active filing activities. Instead, you'll evaluate complex regulatory and scientific content, identify technical inaccuracies, assess document quality and regulatory reasoning, and provide structured feedback that improves AI model performance.
Your pharmaceutical expertise is what matters. AI experience is a plus, not a requirement.
Important Note: This is a freelance, task-based role designed for those seeking supplemental income. It’s essential to understand the nature of freelance work—tasks will be assigned as they become available, and work may be irregular or intermittent.
The Opportunity
As a Regulatory CMC Submission Writer Subject Matter Expert (SME) , you'll serve as a subject matter evaluator, helping assess the quality, accuracy, completeness, and regulatory compliance of Pharmaceutical AI-generated content. …
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