Clinical Trial Manager

Job Summary Medpace is currently looking for a Clinical Trial Manager (CTM) to lead global clinical research studies. Medpace is a scientifically led organization offering full-service solutions for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. The Clinical Trial Manager position is the lead role for multiservice global/regional clinical trials. The CTM interacts with sponsors and sites and manages the timeline and project deliverables (minus finance). This role coordinates all services contracted for the study, leading the cross functional team thru all life cycles of the project (from startup to database lock and closure). CTM will attend bid defense meetings and support business development activities, as needed. This position is office based. Responsibilities •Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations •Serve as primary Sponsor contact for project-specific issues and study deliverables •Maintain in depth knowledge of protocol, therapeutic area, and indication •Provide cross-functional oversight of project team members and deliverables, which includes ensuring all necessary project-specific training is provided •Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable •Develop operational project plans •Manage risk assessment and mitigations •Manage study vendors •Manage site quality, including direct supervision of project Clinical Research Associates (CRA) and monitoring deliverables