• Conducting quality control (QC) review of clinical and regulatory documents, reports, data tables, and slide presentations in support of drug development • Assisting with the oversight of QC projects assigned to contractors and CROs • Performing comprehensive QC reviews of clinical and regulatory documents, reports, data tables, and slide presentations in accordance with predefined, ambitious timelines • Editing documents for grammar, punctuation, consistency, and adherence to internal style guides and regulatory requirements • Collaborating with medical writers, regulatory affairs, and cross-functional teams to resolve discrepancies and ensure document quality • Organizing complex QC projects and providing guidance to other QC reviewers • Supporting authoring process for plain language documents, including but not limited to informed consent forms and plain language protocol synopses • Assisting in maintaining and updating Crinetics Style Guide • Supporting medical writing activities with supervision as needed • Completing other tasks as assigned