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The Individual Gift Officer is responsible for raising private philanthropic gifts to support the patients, programs and research of Cooper University Health Care. The Individual Gift Officer will be responsible to work with assigned areas or institutes of CUHC operations to advance Cooper's vision and goals and will serve as the lead point of contact for fundraising for the assigned area.
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The Project Manager will also be responsible for engaging with the Institutional Review Board (IRB), regulatory affairs, and the Office of Clinical Research to generate documents for AE reporting, continuing review, protocol modifications and study start-up and closeout.
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This involves leveraging Penn electronic systems to improve financial operations and record-keeping (including cross-entity funds transfer according to the location of research services); managing and executing clinical research audit activities (financial) as needed; and structuring the clinical trials finance teams to meet the demands of increasing clinical trial volume, associated regulations, and institutional benchmarks (e.g., study start-up.
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In addition, this position is expected to interact with the institutional investigators, other members of healthcare team, service line members and research participantsfamilies in a manner, which supports the conduct of clinical trials.
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Engaging with the Institutional Review Board (IRB), regulatory affairs, and the Office of Clinical Research. Effective problem-solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible and able to multi-task; demonstrated ability to work as part of a team, as well as independently; knowledge of IRB and human subject research protection regulations, and familiarity with federally-funded research process.
$40 - $45.67 an hourExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nursesPrepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
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Responsibilities PRIMARY FUNCTION:The Clinical Research Coordinator III works under limited supervision and runs portions of clinical trials, assists with orientation and training, obtains signature for informed consent, central lab management, data management, completes expectancy reports, monitors visit preparation, submits low institutional risk trials and tracks TJU IRB submission and approvals.
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They may assist with Institutional Review Board (IRB) filings, sponsor and investigator filings and research related presentations. The research coordinator will assist in the management of multiple clinical trials and will be responsible for study coordination for industry studies, investigator-initiated studies, and multi-center research studies.
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This initiative seeks to support emerging scholars of race and childhood, provide institutional support for racial justice work in the field, and demonstrate the justice and career potential of humanities training through civics-engaged childhood studies.
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The IRB Analyst is part of a research team, which supports the functions and activities of the Institutional Review Board by conducting preliminary reviews of research submissions for completeness and compliance with regulations and institutional policies prior to IRB review.
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