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INSIGHT

<div><div><div><b>WE ARE INSIGHT:</b><br>
<br>
At <b>Insight Hospital and Medical Center- Chicago</b>, we believe there is a better way to provide quality healthcare while achieving health equity. Our Chicago location looks forward to working closely with our neighbors and residents, to build a full-service community hospital in the Bronzeville area of Chicago; creating a comprehensive plan to increase services and meet community needs. With a growing team that is dedicated to delivering world-class service to everyone we meet, it is our mission to deliver the most compassionate, loving, expert, and impactful care in the world to our patients. Be a part of the Insight Chicago team that provides <b>PATIENT CARE SECOND TO NONE! </b>If you would like to be a part of our future team, please apply now!</div><br>
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</div></div><p><b>Job Description: Laboratory Driver / Specimen Courier SHIFT TIMES WILL BE 10:00am-6:30pm</b></p>
<p><b>Position Summary</b></p>
<p>Responsible for the safe and timely transportation of laboratory specimens, supplies, reports, and related materials between client locations, physician offices, outreach accounts, hospitals, and the laboratory. The Laboratory Driver must maintain specimen integrity, follow all safety and confidentiality requirements, and provide excellent customer service to clients and patients. This position requires professionalism, reliability, and adherence to all laboratory, HIPAA, and transportation regulations.</p>
<p><b>Responsibilities</b></p>
<p>1. Pick up laboratory specimens from physician offices, clinics, hospitals, and outreach accounts according to established schedules.</p>
<p>2. Deliver specimens, laboratory supplies, reports, and other materials safely and efficiently.</p>
<p>3. Maintain proper specimen handling, storage, and transportation conditions to ensure specimen integrity.</p>
<p>4. Complete all required logs, manifests, chain-of-custody forms, and transportation documentation accurately.</p>
<p>5. Communicate professionally with laboratory staff, clients, and healthcare providers.</p>
<p>6. Follow all HIPAA, OSHA, laboratory safety, and infection control policies.</p>
<p>7. Perform routine vehicle inspections and report maintenance concerns promptly.</p>
<p>8. Assist with delivery of laboratory supplies and collection materials to client locations.</p>
<p>9. Report transportation delays, specimen issues, or customer concerns to laboratory management immediately.</p>
<p>10. Maintain patient confidentiality at all times.</p>
<div><p><b>Position Qualifications</b></p>
<ul><li>High School Diploma or Equivalent (Required)</li></ul>
<ul><li>Valid Driver's License with a clean driving record (Required)</li></ul>
<ul><li>Previous courier, delivery, healthcare, or laboratory experience (Preferred)</li></ul>
<ul><li>Ability to lift up to 30 pounds and transport laboratory supplies and specimens</li></ul>
<ul><li>Basic knowledge of specimen handling and transportation procedures (Preferred)</li></ul>
<ul><li>Strong communication and customer service skills</li></ul>
<div><div><b>Benefits:</b></div>
<ul><li>Paid Sick Time - effective 90 days after employment</li>
<li>Paid Vacation Time - effective 90 days after employment</li>
<li>Health, vision &amp; dental benefits - eligible at 30 days, following the 1st of the following month</li>
<li>Short and long-term disability and basic life insurance - after 30 days of employment</li>
</ul>
<div><div><b><i>Insight Employees are required to be vaccinated for COVID-19 as a condition of employment, subject to accommodation for medical or sincerely held religious beliefs.</i></b><br>
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<b><i>Insight is an equal opportunity employer and values workplace diversity!</i></b></div></div></div></div></div>

Laboratory Driver/Specimen Courier

<div></div><div><div><b>Job Title:</b> Clinical Research Coordinator III &ndash; Team Lead<br>
<b>Department:</b> Clinical Research Operations<br>
<b>Location:</b> On-site (Insight Hospital &amp; Medical Center Chicago)<br>
<b>Schedule:</b> Full-time, Monday through Friday (8AM-5PM) &ndash;additional flexibility required to meet job requirements</div>
<div><b>Reports To:</b> Director of Clinical Trials</div>
<p></p><div><b>Position Summary</b></div>
<div>The Clinical Research Coordinator III &ndash; Team Lead is a senior-level hybrid role responsible for leading the coordination of complex clinical trials while supervising and mentoring the on-site research team. This position functions as a &ldquo;player/coach,&rdquo; combining direct study coordination with oversight of Clinical Research Coordinators and Clinical Research Assistants. The CRC III &ndash; Team Lead ensures operational excellence, regulatory compliance, and a culture of accountability and continuous improvement.</div>
<div>This role also collaborates closely with the Patient Recruitment department to support enrollment success through candidate prescreening, outreach, and community engagement. In addition, the CRC III &ndash; Team Lead supports regulatory and quality functions directly with the team and in collaboration with centralized regulatory and quality resources.</div>
<p></p><div><b>Core Competencies</b></div>
<ul><li>Advanced knowledge of clinical trial operations, GCP, FDA regulations, and IRB processes</li>
<li>Strong leadership and coaching skills with a collaborative, solutions-oriented mindset</li>
<li>Excellent communication and interpersonal abilities across diverse stakeholders</li>
<li>High attention to detail, time management, and multitasking capabilities</li>
<li>Commitment to quality, compliance, and participant safety</li></ul><br>
<div></div><div><b>Key Responsibilities</b></div>
<div>Study Leadership and Coordination</div>
<ul><li>Serve as lead coordinator on high-priority or complex trials, managing all phases from startup to closeout</li>
<li>Provide backup coverage and operational support for other coordinators during absences or escalations</li>
<li>Ensure protocol adherence, timely data entry, and accurate documentation across assigned studies</li>
</ul><div><b>Team Supervision and Mentorship</b></div>
<ul><li>Supervise and mentor Clinical Research Coordinators I and II and Clinical Research Assistants</li>
<li>Lead onboarding, training, and ongoing development for study staff</li>
<li>Conduct regular team huddles, protocol reviews, and best practice sessions</li>
</ul><div><b>Regulatory and Quality Support</b></div>
<ul><li>Support regulatory and quality functions directly with the team and in collaboration with centralized regulatory and quality resources</li>
<li>Ensure accurate completion, review, and submission of IRB documents, amendments, and safety reports</li>
<li>Maintain essential regulatory files and sponsor communications</li>
<li>Participate in internal audits, monitoring visits, and CAPA implementation</li>
</ul><div><b>Patient Recruitment and Engagement</b></div>
<ul><li>Partner with the Patient Recruitment department to develop and execute enrollment strategies</li>
<li>Conduct candidate prescreening and outreach activities to support recruitment goals</li>
<li>Participate in community engagement efforts to raise awareness and build trust with potential participants</li>
</ul><div><b>Operational Collaboration</b></div>
<ul><li>Serve as liaison between the research team, investigators, sponsors, and institutional departments</li>
<li>Assist in resource planning, visit scheduling, and workload balancing</li>
<li>Contribute to SOP development, workflow optimization, and quality improvement initiatives</li>
</ul>
<p></p><div><b>Qualifications and Requirements</b></div>
<ul><li>Education: Bachelor&rsquo;s degree in life sciences, nursing, or a related field</li>
<li>preferred</li>
<li>Experience: Minimum 4 to 6 years of clinical research coordination experience, including leadership or mentorship responsibilities</li>
<li>Certification: Clinical research certification (e.g., ACRP, SOCRA) preferred</li>
<li>Technical Skills: Proficiency in CTMS, E-Source, E-Reg, EDC platforms, and regulatory systems; strong computer literacy (Microsoft Office Suite, electronic communication tools)</li>
<li>Knowledge Base: Advanced understanding of clinical trial operations, GCP, FDA regulations, and IRB processes</li>
<li>Communication: Excellent written and verbal communication skills; ability to interact effectively with investigators, sponsors, staff, and participants</li>
<li>Leadership: Demonstrated ability to supervise, mentor, and develop staff while fostering accountability and collaboration</li>
<li>Organizational Skills: High attention to detail, time management, and multitasking capabilities; ability to prioritize competing demands</li>
<li>Flexibility: Willingness to adjust schedule to accommodate study visits, meetings, and events that may occur earlier, later, or on weekends</li>
<li>Travel: Ability to travel to training meetings, conferences, satellite sites and other Insight Health System locations as required</li>
<li>Professional Standards: Commitment to quality, compliance, participant safety, and continuous improvement</li></ul></div>

Clinical Research Coordinator III - Team Lead

Join INSIGHT and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

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Laboratory Driver/Specimen Courier

Clinical Research Coordinator III - Team Lead