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, including scheduling and securing locations. Assist with the development of community-facing materials (e.g., consent forms, recruitment flyers, policy briefs) in both English and Spanish. Assist with IRB
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per the different studies run at the CCNP Update IRB protocols for studies as needed Assist in planning and designing new computational psychiatry studies to be run at the CCNP Qualifications Essential
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of the study. 6. Represents the research program at meetings, national and international research consortia. 7. Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and
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, extracting, coding, and analyzing clinical research data Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry
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forms, abstracts and manuscripts. Creates IRB and/or IACUC protocols, submits for review/approval and maintains correspondence with sponsoring agency, IRB and collaborative institutions. Maintains
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collection, communications with IRB, data management, creating tables and figures, benchmarking the data with external public data sets such as the National Health Interview Survey, California Health Interview
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report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research
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other databases. Ensures regulatory documents are properly completed and filed, serves as a liaison between investigators, IRB, REDCap, and other relevant healthcare professionals who are part of
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with UIC information technology research infrastructures, e.g. REDCap, UIC Advanced Cyberinfrastructure for Education and Research (ACER), Azure SCE, UIC IRB and UI Health data regulations and policies
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including Institutional Review Board (IRB) & federal or industry sponsor processes and requirements; ACRP (Assn of Clinical Research Professionals) or SOCRA (Society of Clinical Research Associates