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About the Role
Elevate your career with Apsida Life Science as a Principal Regulatory Writer, supporting North American clients in the pharmaceutical sector. This role involves strategic regulatory writing with a focus on CTD Module 2 submissions.
Apsida Life Science is looking for an experienced Principal Regulatory Writer to enhance their North American presence. This position requires a minimum of five years in regulatory writing, specifically with CTD Module 2 submissions. You'll provide scientific expertise, manage client accounts, and ensure the accuracy of critical documentation for diverse therapeutic projects.
Key Responsibilities:
• Manage technical aspects of designated client accounts
• Lead complex programs for submissions, focusing on CTD Module 2
• Deliver clear, accurate, and well-written regulatory documents
• Support budget development and reviews as necessary
Requirements:
• Degree in Life Science or related field
• 5+ years of experience in Regulatory Wr...
Apsida Life Science is looking for an experienced Principal Regulatory Writer to enhance their North American presence. This position requires a minimum of five years in regulatory writing, specifically with CTD Module 2 submissions. You'll provide scientific expertise, manage client accounts, and ensure the accuracy of critical documentation for diverse therapeutic projects.
Key Responsibilities:
• Manage technical aspects of designated client accounts
• Lead complex programs for submissions, focusing on CTD Module 2
• Deliver clear, accurate, and well-written regulatory documents
• Support budget development and reviews as necessary
Requirements:
• Degree in Life Science or related field
• 5+ years of experience in Regulatory Wr...
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