<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 the necessary Care Access and protocol specific training</span><span class="NormalTextRun SCXW111068282 BCX0">s</span></span></li><li><span class="EOP SCXW111068282 BCX0" data-ccp-props="{}"><span class="TextRun SCXW219650447 BCX0" lang="EN-US" data-contrast="auto"><span class="NormalTextRun SCXW219650447 BCX0">C</span><span class="NormalTextRun SCXW219650447 BCX0">omply with</span><span class="NormalTextRun SCXW219650447 BCX0"> ICH GCP (International Conference on Harmonization – Good Clinical Practice) and all applicable regulatory requirements</span></span> </span></li><li><span class="EOP SCXW111068282 BCX0" data-ccp-props="{}"><span class="EOP SCXW219650447 BCX0" data-ccp-props="{}">Participate in monitoring visits and sponsor meetings; allow monitoring and auditing by sponsors and inspection by appropriate regulatory agencies </span></span> </li></ul></div><div><h3><strong>The Expertise Required</strong></h3><ul><li>Excellent written and verbal communication skills </li><li>Ability to effectively prioritize tasks in a fast-paced environment </li><li>Attention to detail and ability to maintain confidentiality when handling sensitive information. </li><li>Critical thinking, dynamic problem-solving skills </li></ul><h3 class="text-body text-muted"><strong>Certifications/Licenses, Education, and Experience</strong></h3><ul><li><span data-contrast="auto">Minimum Education:</span><ul><li><span class="TextRun MacChromeBold SCXW267535968 BCX0" lang="EN" data-contrast="auto"><span class="NormalTextRun SCXW267535968 BCX0">M</span><span class="NormalTextRun SCXW267535968 BCX0">D or DO with an active, unrestricted </span><span class="NormalTextRun SCXW267535968 BCX0">medical</span><span class="NormalTextRun SCXW267535968 BCX0"> license (medical license must be valid in the state in which the research is conducted)</span></span></li></ul></li><li><span data-contrast="auto">Minimum Experience:</span><ul><li><span data-contrast="auto">Previous experience as a Principal Investigator is required; 2 years prior experience as a Principal Investigator or Sub-Investigator, preferred</span><span data-ccp-props="{}"> </span></li><li><span data-contrast="auto">Training and certification in Good Clinical Practice (GCP)</span><span data-ccp-props="{}"> </span></li></ul></li></ul><h3><strong style="font-size: 14px;">How We Work Together</strong></h3></div></div><div><ul><li><strong>Location</strong>: Remote within the United States. This role requires 100% of work to be performed in a remote office environment.</li><li><strong>Travel</strong>: This is a remote position with less than 10% travel requirements. Occasional planned travel may be required as part of the role.</li><li><strong>Physical demands associated with this position Include</strong>: The ability to use keyboards and other computer equipment.</li></ul><p style="text-align: center;">The expected pay range for this role is $200,000 - $400,000 USD per year for full time team members.</p><h3><strong>Benefits & Perks (US Full Time Employees)</strong></h3><ul><li>Paid Time Off (PTO) and Company Paid Holidays</li><li>100% Employer paid medical, dental, and vision insurance plan options</li><li>Health Savings Account and Flexible Spending Accounts</li><li>Bi-weekly HSA employer contribution</li><li>Company paid Short-Term Disability and Long-Term Disability</li><li>401(k) Retirement Plan, with Company Match </li></ul><div style="text-align: left;"> </div><div style="text-align: left;"><h3><strong>Mandatory Employer Disclosures</strong></h3></div><div style="text-align: left;"><strong>Notice to Illinois applicants:</strong> Applicants are not obligated to disclose expunged juvenile records or adjudication, arrest, or conviction.<br><strong>Notice to Connecticut applicants:</strong> Care Access may require applicants to submit to a urinalysis drug test in connection with an application for employment.<br><strong>Notice to Arizona, Georgia, Indiana, and North Dakota applicants:</strong> Care Access complies with applicable laws prohibiting smoking in and around places of employment.<br><strong>Notice to Massachusetts applicants:</strong> It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.<br><strong>Notice to Rhode Island applicants: </strong>Care Access complies with Rhode Island law prohibiting smoking in enclosed areas within places of employment. Care Access is also subject to is subject to Chapters 29–38 of Title 28 of the Rhode Island General Laws.<br><strong>Notice to Maryland applicants: UNDER MARYLAND LAW, AN EMPLOYER MAY NOT REQUIRE OR DEMAND, AS A CONDITION OF EMPLOYMENT, PROSPECTIVE EMPLOYMENT, OR CONTINUED EMPLOYMENT, THAT AN INDIVIDUAL SUBMIT TO OR TAKE A LIE DETECTOR OR SIMILAR TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT EXCEEDING $100. </strong></div><div style="text-align: left;"> </div><div style="text-align: left;"><p>#LI-Remote</p></div></div><div class="content-conclusion"><p><strong>Diversity & Inclusion</strong></p><p>We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. </p><p>We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.</p><p>Care Access is unable to sponsor work visas at this time.</p><p>If you need an accommodation to apply for a role with Care Access, please reach out to: <a href="mailto:TalentAcquisition@careaccess.com">TalentAcquisition@careaccess.com</a></p><p data-olk-copy-source="MessageBody"> </p></div>