Sort by
Refine Your Search
-
, protocols, amendments, correspondence and serious adverse event reports. Performs extensive audits and monitoring visits to determine protocol compliance, including the consent process and eligibility
-
concepts and details to the research subjects, participates in the informed consent process, enrolls, and coordinates care of subjects in compliance with protocol requirements. The CSC may provide education
-
, RT-PCR, and cytotoxicity assays, under minimal supervision. You will provide supervision and training to junior team members and support the qualification and validation of manufacturing processes and
-
research-related documents. You will serve as a project manager, navigating the regulatory review process for each research study, ushering manuscripts through the submission and revision process, and
-
tissue collection), DNA extraction, PCR analysis, histological techniques, fluorescent microscopy, computer skills (word processing, email, spreadsheet management, adobe photoshop, Image J), and lab
-
strategy for identifying potentially eligible patients for each study. The CRN presents trial concepts and details to the research subjects, participates in the informed consent process, enrolls, and
-
, ligation, suture), vascular/endothelial biology, RNA/chromatin biology, immunohistochemistry, immunology, sequencing analysis and bioinformatics, flow cytometry and imaging-based analyses, tissue processing
-
needed. Provide education and training to clinical staff on research protocols and procedures. Develop study-specific tools and manage biological specimen collection, processing, and shipping. Maintain
-
and Senior QA Associate in achieving compliance with all Federal and State laws and regulations and other accrediting agency requirements in the collection, processing, preparation, and distribution
-
. Ensure the consent process is performed in compliance with institutional, FDA, IRB, clinical trial sponsor and other applicable regulations.