The Research Assistant will support clinical trial operations by managing project documentation, performing quality control reviews, and assisting with data management tasks. They will also serve as a study coordinator for select projects and facilitate communication between study sites and the research team.
Manage clinical trial operations including site identification, regulatory compliance, and the development of essential study documents. Oversee project timelines, vendor contracts, and multidisciplinary teams to ensure high-quality project deliverables.
The Sr. Clinical Operations Manager serves as the primary contact for industry-sponsored clinical trials, overseeing project scope, timelines, and deliverables. They are responsible for managing site identification, regulatory compliance, vendor contracts, and mentoring other Clinical Operations Managers.
Oversee clinical operations management for industry-sponsored trials, including defining project scope, timelines, and deliverables from initiation to close-out. Manage multidisciplinary teams and provide operational support for biostatistics, programming, and endpoint specialty services.
