Job Description
Elevate your career as a Principal Regulatory Writer with Apsida Life Science, supporting clients across North America. This role emphasizes strategic projects and complex CTD Module 2 submissions.
Apsida Life Science is seeking an experienced Principal Regulatory Writer based in Canada or the US. You will lead high-complexity submissions and manage deliverables for designated client accounts. This position offers the flexibility of a 0.8 FTE working model while contributing to diverse therapeutic projects for global pharmaceutical organizations.
Key Responsibilities:
• Manage specific project deliverables for clients
• Lead submissions, particularly CTD Module 2 tasks
• Ensure the delivery of accurate, clear documents
• Provide technical expertise throughout the project
• Support project budgeting alongside management team
Requirements:
• Degree in Life Science or related area
• Minimum 5+ years in Regula...
Apsida Life Science is seeking an experienced Principal Regulatory Writer based in Canada or the US. You will lead high-complexity submissions and manage deliverables for designated client accounts. This position offers the flexibility of a 0.8 FTE working model while contributing to diverse therapeutic projects for global pharmaceutical organizations.
Key Responsibilities:
• Manage specific project deliverables for clients
• Lead submissions, particularly CTD Module 2 tasks
• Ensure the delivery of accurate, clear documents
• Provide technical expertise throughout the project
• Support project budgeting alongside management team
Requirements:
• Degree in Life Science or related area
• Minimum 5+ years in Regula...
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