• Perform rigorous quality assessments of the following documents: clinical study reports; original protocols, as well as global and country-specific protocol amendments, investigator's brochures, and summary documents, such as clinical overviews (m2.5), summaries of clinical pharmacology studies (m2.7.2), summaries of clinical efficacy (m2.7.3), and summaries of clinical safety (m2.7.4)• Edit documents for grammatical and formatting errors, alignment with internal Style Guide, hyperlink accuracy, and data source verification• Lead project to provide just-in-time training videos on QC processes by drafting and recording videos• Create and update internal tools such as presentations, QC handbook, and onboarding plan to clarify the role of the QC Team to external teams and new hires, as well as the QC assessment used to evaluate candidates' skill sets when hiring• Work effectively within the Medical Writing group to produce high-quality, scientifically accurate documents under strict timelines and to ensure consistency between related documentsBeiGene, Ltd. is a biotechnology company that specializes in the discovery, development, and commercialization of innovative, molecularly targeted immuno-oncology drugs for the treatment of cancer.