Principal Investigator (Virtual)

<div class="content-intro"><p><strong>About Care Access</strong></p> <p>Care Access is working to make the future of health better for all. <strong>With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. </strong>We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, <strong>and contribute to the medical breakthroughs of tomorrow.</strong></p> <p>With programs like <em>Future of Medicine</em>, which makes advanced health screenings and research opportunities accessible to communities worldwide, and <em>Difference Makers</em>, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.</p> <p>To learn more about Care Access, visit <a href="http://www.careaccess.com/">www.CareAccess.com</a>.</p></div><div> <h3><strong>How This Role Makes a Difference</strong></h3> <p>We are seeking a highly skilled and experienced virtual <strong>Principal Investigator</strong> to join our team. As the Principal Investigator, you will be responsible for oversight of all clinical trials according to study protocols, company processes, and GCP. <strong>Please note this is a part-time role.</strong></p> <div> <h3><strong>How You'll Make An Impact</strong></h3> <ul> <li><span data-contrast="auto">Provide overall medical oversight and medical review of protocols in conformance with good clinical practice</span><span data-ccp-props="{}"> </span> <ul> <li><span data-contrast="auto">Review sponsor provided safety reports.</span><span data-contrast="auto"> </span><span data-ccp-props="{}"> </span></li> <li><span data-contrast="auto">Review and maintain accurate case report forms. </span><span data-ccp-props="{}"> </span></li> </ul> </li> <li>Ensure that the safety and well-being of all participants in the study at the trial site are protected <ul> <li>Assess subject response to therapy, evaluate and address adverse experiences </li> </ul> </li> <li><span class="TextRun SCXW136497904 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW136497904 BCX0">Perform physical assessments, examinations and study procedures as required by study protocols</span></span><span class="EOP SCXW136497904 BCX0" data-ccp-props="{}"> </span></li> <li><span data-contrast="auto">Train Sub-Investigators and study staff members on protocol and protocol specific procedures. Provide medical support to sub-investigators and study staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. </span><span data-ccp-props="{}"> </span> <ul> <li><span data-contrast="auto">Review the inclusion/exclusion criteria, endpoint criteria, and investigational product use with the internal research team. </span><span data-ccp-props="{}"> </span></li> </ul> </li> <li><span class="TextRun SCXW111068282 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW111068282 BCX0">Complete