Job Summary:

Provides guidance across teams and in research proposal preparation and submission for portfolios of various clinical trials, as applicable. Reviews, edits, and ensures accurate compilation of study documentation sent to regulatory bodies (e.g., IRB) for pre-implementation review and approval. May oversee clinical trials activities and research lab operations. Guides the planning of strategies for monitoring progress on the timeliness, accuracy, and completion of documentation for all research activities (e.g., consent forms, reports). Influences the development of new strategies for developing quality control and/or assurance measures and provides feedback to research staff and management. Assesses and ensures staff are educating on protocol implementation, documentation procedures, clinical best practices, or timeliness of submissions. Sets and manages the reviewing and drafting of contract proposals across teams, and forecasts and plans budgets for internally an...