About the Role
<h4>About Us</h4><p>Here at Baylor Scott & White Health we promote the well-being of all individuals, families, and communities. Baylor Scott and White is the largest not-for-profit healthcare system in Texas that empowers you to live well.</p><p>Our Core Values are:</p><ul><li>We serve faithfully by doing what's right with a joyful heart.</li><li>We never settle by constantly striving for better.</li><li>We are in it together by supporting one another and those we serve.</li><li>We make an impact by taking initiative and delivering exceptional experience.</li></ul><h4>Benefits</h4><p>Our benefits are designed to help you live well no matter where you are on your journey. For full details on coverage and eligibility, visit the Baylor Scott & White Benefits Hub to explore our offerings, which may include:</p><ul><li>Immediate eligibility for health and welfare benefits</li><li>401(k) savings plan with dollar-for-dollar match up to 5%</li><li>Tuition Reimbursement</li><li>PTO accrual beginning Day 1</li></ul><p><em>Note: Benefits may vary based upon position type and/or level.</em></p><h4>Job Summary</h4><p>The Clinical Research Coordinator 2 helps Principal Investigators conduct clinical trials. This includes all phases from pre-study implementation to study closure, following federal, state, and Institutional guidelines.</p><h4>Essential Functions of the Role</h4><ul><li>Reviews new protocols and materials from Study Sponsors. Provides input to PIs and clinical managers on clinical and research issues. Establishes financial and clinical feasibility.</li><li>Coordinates research project protocols with departments by interacting with PIs, clinical managers, and supervisors. Provides in-service education for healthcare professionals. Works with Pharmacy to ensure smooth project flow.</li><li>Reports to the Institutional Review Board (IRB), completing IRB review reports and assisting with drug accountability.</li><li>Develops research study budgets for new clinical trials and assists in the completion of all applicable research billing compliance procedures.</li><li>Coordinates study-monitoring visits. Completes and submits monthly invoices for applicable patient care charges covered by funded research studies.</li><li>Participates in data testing, writing and submitting manuscripts and abstracts for publication, as appropriate.</li><li>Develops, implements and administers Clinical Research policies and procedures.</li><li>Unites with quality audits.</li></ul><h4>Key Success Factors</h4><ul><li>Research certification and other certifications per specialty area preferred.</li><li>Proven written and oral communication skills.</li><li>Proven computer skills, including Microsoft Office.</li><li>Ability to manage time reactive projects in order to meet deadlines.</li><li>Exceptional ability to establish and maintain effective working relationships.</li><li>Ability to autonomously operationalize and coordinate large or complex studies from start to finish.</li><li>Ability to autonomously work across functional departments within BSWRI.</li><li>Proven critical thinking and problem-solving skills; ability to troubleshoot study challenges.</li><li>Ability to work within a team, including training of junior staff.</li></ul><h4>Belonging Statement</h4><p>We believe that all people should feel welcomed, valued and supported.</p><p><b>QUALIFICATIONS</b></p><ul><li>EDUCATION - Bachelor's or 4 years of work experience above the minimum qualification</li><li>EXPERIENCE - 2 Years of Experience</li><li>CERTIFICATION/LICENSE/REGISTRATION -</li></ul><p>Cert Clinical Research Assoc (CCRA), Cert Clinical Research Coord (CCRC), CCRP-Cert Clnl Research Prof (CCRP-RES): Obtain research certification related to your work area within one year.</p>