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, entry, and tracking; reviews medical or research data for study eligibility; and helps prepare documentation for compliance and reporting. Contributes to reviews to the IRB, literature reviews, reports
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be expected to prepare Institutional Review Board (IRB) applications and local school district applications for review of planned research. This individual will also facilitate weekly meetings
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subaward agreements, track expenditures, monitorproject timelines and milestones, and prepare research reports for sponsors. Maintain IRB protocols and modifications, ensure compliance with human subjects
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inference methods. • Develop statistical analysis plans (SAPs) for grants, IRB submissions, and evaluation contracts. Data Management & Collaboration • Work closely with the Data Engineer/IT Project Manager
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: Oversee the informed consent process, ensuring that participants fully understand the Study procedures, risks, and benefits. Document the consent process in compliance with IRB guidelines and GCP standards
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defined by the IRB. These studies may include protocols with blood draws, repositories, survey studies, simple observational studies, and studies that do not involve investigational products or devices. Not
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to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations Assists with coordinating and preparing for external quality
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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