Senior Medical Writer: CSR & Regulatory Submissions Lead

Sagimet Biosciences is seeking an experienced Medical Writer to lead the preparation of clinical study reports and regulatory submissions for Phase II/III programs. You will collaborate with Clinical Operations, Biostatistics, and Regulatory Affairs to ensure submission-ready documents meeting ICH, FDA, and EMA standards.

The role requires a strong writing background, cross-functional collaboration, and the ability to translate complex data into clear, compliant documents that support regulatory

For the Senior Medical Writer: CSR & Regulatory Submissions Lead position at Sagimet Biosciences, we are reviewing applications now.

Take a moment to read everything above and see whether this role is right for you.

This posting is for the Senior Medical Writer: CSR & Regulatory Submissions Lead role at Sagimet Biosciences, based in Foster City, CA, United States.

We are looking to fill the Senior Medical Writer: CSR & Regulatory Submissions Lead position at Sagimet Biosciences in Foster City, CA, United States.