Clinical Medical Writer – Regulatory Documents

A global biotechnology company is seeking a Medical Writer 1 to draft and edit clinical study documents and provide regulatory support. The ideal candidate has a Bachelor's or higher degree in a scientific field, with up to 2 years of medical writing experience and strong knowledge of regulatory standards. This role involves collaboration with cross-functional teams to ensure high-quality documentation for clinical studies, contributing to the advancement of human health. #J-18808-Ljbffr