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screening potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process. Maintain accurate source documents
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. 2 years prior experience with research budgets and/or hospital billing processes. Working knowledge of the Medicare clinical trial policy. Must have experience working closely with physicians and/or
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Clinical Research Coordinator III-Part Time Med-Neurological Surgery - Pennsylvania-Pittsburgh - (25002443) Job Summary Prepares grant applications, manuscripts, Institutional Review Board (IRB
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wellness center, the Scheduling & Events Coordinator will directly contribute to and support the planning, opening, and operation of the new facility. Major responsibilities include manage and oversee
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study activity. Oversees collection and processing of lab results and ensures compliance with protocol and regulatory standards. Performs general laboratory duties and guides staff. Essential Functions
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account activity, performs internal audits, resolves complex issues, and provides policy and procedure interpretation. Prepares complex government reports and reviews routine reports. Facilitates accounting
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computer, problem solving and organizational skills. Work must be accurate, complete and timely. Experience with Outlook, Teams, Zoom, Microsoft Suite, Excel, PowerPoint and Endnote is a plus. Physical
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computer, problem solving and organizational skills. Work must be accurate, complete and timely. Experience with Outlook, Teams, Zoom, Microsoft Suite, Excel, PowerPoint and Endnote is a plus. Physical
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of infectious materials, and comfort in handling experimental animals. Candidates must be able to learn and retain a variety of skills required for experimentation, including operation of laboratory equipment and
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, and monitors very complex grants, contracts, subcontracts, and budgets. Prepares complex government applications and reports and interprets policy and procedure. Monitors account activity, performs