
The Associate Director of Medical Writing leads the development of critical regulatory and clinical documents for Structure Therapeutics, a biotech firm focused on innovative small molecule medicines for chronic diseases. Key responsibilities include authoring and finalizing high-quality documents such as clinical study protocols and briefing documents, conducting rigorous quality control reviews to ensure regulatory compliance, and managing multiple projects across global cross-functional teams. The role offers the opportunity to drive strategic writing initiatives within a fast-paced, collaborative environment that values scientific excellence. While the position is based in Southern California with a requirement for monthly on-site attendance, it supports a dynamic culture of innovation and provides significant professional growth through interaction with international teams and leadership in the drug development process.






















