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operations of a clinical research team conducting multiple, complex oncology clinical trials, including studies involving Investigational Products (IP). You will partner closely with Principal Investigators
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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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train Clinical Research Specialists (CRSs) in these tasks. Work Performed Research Operations Under supervision, assists with managing investigational products (IP) including arrival, storage, and
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-on coordination for multiple, complex oncology clinical trials, including studies involving Investigational Products (IP). You will play a critical role in advancing cancer research by supporting participants
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development, submission, and maintenance of relevant documentation. Addresses FDA review and/or potential hold issues in collaboration with the Principal Investigator (PI). May train or oversee others
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, compilation, documentation, and analysis of clinical research data. May oversee the work of junior staff and train or mentor others in clinical research tasks. Provides and documents professional nursing
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. Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and SOPs. May train others in these policies and processes. Is responsible