YO AI Labs is seeking an experienced Medical Writer/Clinical Document Author for a remote contracting role. You will develop and review regulatory documents, ensuring scientific accuracy and regulatory compliance across CSRs and related submissions.
Key responsibilities include interpreting clinical protocols, verifying data with TFLs, and collaborating with cross-functional teams. Experience with ICH E3/E2F/E2C and eCTD is essential, with oncology experience being a plus.
#J-18808-LjbffrRemote Regulatory Medical Writer — CSR & ICH Expert in washington at Unknown Company
This position is listed as contract and able to be worked remotely.