_:n52362a28a89246de9e5cdfff31017d4axb0
<http://schema.org/responsibilities>
"<p style=\"margin: 0px; padding: 0px; color: windowtext;\"><span style=\"font-family: helvetica; font-size: 12pt;\"><strong><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">The essential&nbsp;duties and&nbsp;responsibilities:</span></strong><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></p><ul><li><span style=\"font-family: helvetica; font-size: 12pt;\"><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">Work closely with physicians to identify and screen potential patients for clinical trial participation</span><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></li><li><span style=\"font-family: helvetica; font-size: 12pt;\"><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">Present trial concepts and details to oncology patients while conducting the informed consent process.</span><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></li><li><span style=\"font-family: helvetica; font-size: 12pt;\"><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">Assess patients for adverse events and/or changes in condition&nbsp;</span><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></li><li><span style=\"font-family: helvetica; font-size: 12pt;\"><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">Provide staff and patient education regarding the management and administration of investigational product</span><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></li><li><span style=\"font-family: helvetica; font-size: 12pt;\"><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">Ensure accurate and timely documentation and data entry to meet trial requirements</span><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></li><li><span style=\"font-family: helvetica; font-size: 12pt;\"><span style=\"margin: 0px; padding: 0px;\" data-contrast=\"auto\">Serve as a liaison between clinic departments to ensure proper trial conduct</span><span style=\"margin: 0px; padding: 0px;\" data-ccp-props=\"{&quot;134233279&quot;:true,&quot;201341983&quot;:0,&quot;335559739&quot;:200,&quot;335559740&quot;:276}\">&nbsp;</span></span></li></ul>"
<https://careers.usoncology.com/main/jobs/28262?lang=en-us>