Chandllor H.

Clinical Trial Associate @Denali Therapeutics

Provide high quality assistance in managing and overseeing clinical trials according to ICH GCP and applicable regulatory requirements and SOPs - Contribute to the development of study specific documents, plans, and tools (e.g. ICFs, pharmacy manual, dosing diaries, etc.)- Help oversee data collection processes, verifying the accuracy and completeness of data through monitoring visits and remote data review- Maintain effective communication with investigational sites, investigators, and study teams, addressing queries and providing guidance- Participate in internal and external audits and inspections, helping to ensure trial processes and documentation meet quality standards- Collaborate with cross-functional teams, including data management, biostatistics, and medical affairs, to support study activities.