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and NIH/FDA research guidelines Regulatory/IRB procedures and study operations Opportunities for data analysis, grant writing, and abstract preparation Mentoring Through involvement in ongoing
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opportunities to be trained in clinical trials, conduct literature reviews, participate in manuscript writing and preparation, and participate in maintaining Institutional Review Board (IRB) documents. This
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contributions, and conference presentations. Adheres rigorously to institutional review board (IRB) protocols, HIPAA regulations, and ethical guidelines governing patient data in research. Maintains
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include: Editing IRB language as needed by submitting amendments Creating recruitment flyers using Canva Recruiting participants for interviews and focus groups Conducting focus groups and interviews
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. · Manage IRB submissions, reporting and management of studies. · Mentoring undergraduate and graduate students in their work on grant-funded projects. · Active dissemination of research in the
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, culturing, and characterizing primary human or animal cells from tissues or biological samples. • Experience developing, submitting, and maintaining Institutional Review Board (IRB) protocols and
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collection Experience with virtual reality (VR) or simulation-based research Experience with machine learning, deep learning, or multimodal data analysis Experience conducting human-subject research and IRB
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participants’ database, conducting various analytical work, compliance checking for NGOs’ data collection, supporting administrative duties (e.g. procurement, IRB, etc.) and performing any other
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participants’ database, conducting various analytical work, compliance checking for NGOs’ data collection, supporting administrative duties (e.g. procurement, IRB, etc.) and performing any other
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initiatives. Develops research protocols that includes IRB submissions and amendments. Contributes to coordinate multicenter clinical research studies. Works collaboratively and professionally within