Senior Regulatory Medical Writer — FDA Submissions Expert

Immix Biopharma, Inc. seeks a Senior Medical Writer to prepare, review, and edit regulatory documents for FDA submissions, ensuring accuracy and regulatory compliance across IND, NDA, and BLA programs.

You will collaborate with clinical, regulatory, and scientific teams, manage multiple writing projects and timelines, and contribute strategic regulatory writing input throughout the development lifecycle. A life sciences degree and 5+ years in regulatory writing are required.

We have an opening for a Senior Regulatory Medical Writer — FDA Submissions Expert in Los Angeles, CA, United States within Marketing & Media.

The Senior Regulatory Medical Writer — FDA Submissions Expert role at Immix Biopharma (Nasdaq: IMMX) is now open for applications in Los Angeles, CA, United States.

Join us at Immix Biopharma (Nasdaq: IMMX) as our next Senior Regulatory Medical Writer — FDA Submissions Expert in Los Angeles, CA, United States.