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. You will provide leadership and coordination for multiple, complex oncology clinical trials—including investigational products (IP)—within the Duke Cancer Institute’s Brain Tumor Clinical Research
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with study documentation, protocol submissions, and standard operating procedures (SOPs). Is responsible for all aspects of managing and documenting Investigational Product (IP); including arrival
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study documentation, protocol submissions, and SOPs. May train others in these policies and processes. Is responsible for all aspects of managing and documenting Investigational Product (IP); including
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Investigational Product (IP); including arrival, storage, tracking, and provision to research participants. Serves as the primary liaison with sponsors, IDS, and other parties as necessary. Follows protocol schema
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of managing and documenting investigational product (IP); including arrival, storage, tracking, and provision to research participants. Serves as the primary liaison with sponsors, Investigational Drug Service
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‑up on review or hold issues. Apply knowledge of institutional and regulatory processes in protocol submissions, documentation, and SOP development. Manage investigational product (IP), including
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: Under supervision, assists with managing investigational products (IP) including arrival, storage, and handling (requisitions, inventory, and reordering). Under supervision, prepares for study monitoring
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execution and approval processes. • Oversee investigational product (IP) management for multiple studies, including documentation, handling methods, and compliance. • Develop, optimize, and manage systems
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and procedures. May delegate tasks and supervise the activities of other licensed and unlicensed research staff. Is responsible for all aspects of managing and documenting Investigational Product (IP
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. May delegate tasks and supervise the activities of other licensed and unlicensed research staff. Is responsible for all aspects of managing and documenting Investigational Product (IP); including