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to appropriate committees, ensuring timely completion of the approval process. Keep stakeholders informed of protocol approval and activation issues, including regulatory status updates for sponsors and
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accurate documentation throughout the research process. Compile and submit data according to protocol guidelines, ensuring compliance with study requirements. Actively recruit patients for studies and assist
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expected medical necessity, and assigning costs for clinical and non-clinical components of each trial. Must understand the clinical trial and corresponding protocol in order to determine coding and charge
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negotiation and development, and performing necessary performance management to ensure project success within defined cost parameters. Process development and implementation Designs and develops systems
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to the research subjects, participates in the informed consent process, enrolls, and coordinates care of subjects in compliance with protocol requirements. The CRN may provide teaching on investigational agents
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in to IRB clinical trials. Assess and document signs and symptoms of illness, reactions to treatment, changes in physical or psychological condition and general appearance in accordance with the IRB
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researchers under OCPD Senior Manager's guidance to develop, write, and edit diverse clinical research protocols. Shape the future of medical research in a dynamic environment. The position is fully remote. As
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data reporting requirements. Review and process invoices from sub-sites. Regulatory Responsibilities for Participating Sites: Manage deviation, adverse event, and unanticipated problem reporting. Systems
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targeted gene modification of human HSPC and iPSC, on strategies to modulate stemness and on the development of niche-mimetics. · Interact with the Process Development team and will participate in
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. For more information on Dr. Schones’ research please visit here . · PhD or M.D. in biology, computer science, biomedical engineering, physics or other related discipline. · Excellent