YO AI Labs is seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing.
Key responsibilities include authoring and reviewing CSRs and regulatory submissions, interpreting clinical protocols per ICH guidelines, and ensuring accuracy with source data, TFLs, and study docs; there is collaboration with cross-functional teams and
#J-18808-LjbffrRemote Medical Writer for Regulatory CSR & ICH Documents in california at Unknown Company
This position is listed as full time and onsite.