Clinical Research Coordinator, RN

About this role

<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><h3><strong>How This Role Makes a Difference</strong></h3> <p><span class="TextRun SCXW111946875 BCX0" lang="EN" data-contrast="none"><span class="NormalTextRun SCXW111946875 BCX0" data-ccp-charstyle="normaltextrun" data-ccp-charstyle-defn="{"ObjectId":"ac0262f4-8a9e-5820-b908-2d943c5f7113|1","ClassId":1073872969,"Properties":[469777841,"Arial",469777842,"Arial",469777843,"Arial",469777844,"Arial",469769226,"Arial",268442635,"22",469775450,"normaltextrun",201340122,"1",134233614,"true",469778129,"normaltextrun",335572020,"1",469778324,"Default Paragraph Font"]}">The <strong>Clinical Research Coordinator, RN</strong> conducts delegated clinical tasks and monitoring of research participants </span><span class="NormalTextRun SCXW111946875 BCX0" data-ccp-charstyle="normaltextrun">in accordance with</span><span class="NormalTextRun SCXW111946875 BCX0" data-ccp-charstyle="normaltextrun"> Good Clinical Practices (GCP), ensuring protocol and regulatory compliance.</span></span><span class="TextRun SCXW111946875 BCX0" lang="EN-US" data-contrast="none"><span class="NormalTextRun SCXW111946875 BCX0" data-ccp-charstyle="eop" data-ccp-charstyle-defn="{"ObjectId":"920dbcde-2834-5e15-a5fa-062170b236ba|1","ClassId":1073872969,"Properties":[469777841,"Arial",469777842,"Arial",469777843,"Arial",469777844,"Arial",469769226,"Arial",268442635,"22",469775450,"eop",201340122,"1",134233614,"true",469778129,"eop",335572020,"1",469778324,"Default Paragraph Font"]}"> </span></span><span class="EOP SCXW111946875 BCX0" data-ccp-props="{"201341983":0,"335559740":240}"> </span></p> <div> <h3><strong>How You'll Make An Impact</strong></h3> <ul> <li>Ability to understand and follow institutional SOPs.  </li> <li>Review and assess protocol (including amendments) for clarity, logistical feasibility  </li> <li>Ensure that all training and study requirements are met prior to trial conduct.  </li> <li>Discuss study medication, required procedures, eligibility criteria and impact on office flow with Investigator and site staff.  </li> <li>Assist with planning and creation of appropriate recruitment materials.  </li> <li>Assist in development of recruitment plan and obtain listing of potential candidates to contact from subject database.  </li> <li>Actively work with recruitment team in calling and recruiting subjects   </li> <li>Attend Investigator meetings as required.   </li> <li>Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.  </li> <li>Assist in the creation and review of source documents.  </li> <li>Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)  </li> <li><strong>Study Management:</strong>   <ul> <li>Prioritize activities with specific regard to protocol timelines  </li> <li>Maintain adherence to Health Canada Division 5 regulations and ICH guidelines in all aspects of conducting clinical trials.  </li> <li>Maintain effective relationships with study participants and other care Access Research personnel.  </li> <li>Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and…