Gilead Sciences

Manager

• Coordinating and supervising all aspects of a clinical study
• Monitors clinical trial sites
• Assists Clinical Program Manager in overall study management
• Drafts and coordinates review of relevant documents
• Maintains study timelines
• Contributes to development of study budget
• Manage CROs/vendors
• Ensures effectiveness of site budget/contract process

Clinical Trials Manager

• Coordinating and supervising all aspects of a clinical study
• Monitors clinical trial sites
• Assists Clinical Program Manager in overall study management
• Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports
• Maintains study timelines
• Contributes to development of study budget
• Contributes to development of RFPs and participate in selection of CROs/vendors
• Manage CROs/vendors
• Coordinates review of data listings and preparation of interim/final clinical study reports
• May contribute to development of abstracts, presentations, and manuscripts
• Ensures effectiveness of site budget/contract process
• May be asked to train CROs, vendors, investigators, and study coordinators on study requirements