About Us

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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.

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Our Core Values are:

\n\nWe serve faithfully by doing what's right with a joyful heart.\nWe never settle by constantly striving for better.\nWe are in it together by supporting one another and those we serve.\nWe make an impact by taking initiative and delivering exceptional experience.\n\n

Benefits

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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:

\n\nEligibility on day 1 for all benefits\nDollar-for-dollar 401(k) match, up to 5%\nDebt-free tuition assistance, offering access to many no-cost and low-cost degrees, certificates and more\nImmediate access to time off benefits\n\n

At Baylor Scott & White Health, your well-being is our top priority.

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Note: Benefits may vary based on position type and/or level

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JOB SUMMARY

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The Clinical Research Coordinator I assists various Principal Investigators (PI), through delegated authority, in conducting clinical trials during all phases of trials including pre-study implementation through study closure per federal, state and Institutional guidelines. This position will learn to assist Principal Investigators on more complex studies and seek guidance from more senior roles when needed

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ESSENTIAL FUNCTIONS OF THE ROLE

\n\nConducting patient facing clinical research visits for various interventional and complex pulmonary clinical trials.\nManage assigned clinical trials during all phases of study execution including Study Operationalizing (source document creation, workflow, managing inventory, etc), Study Enrollment & Follow Up (executing patient visits, managing data queries, etc), and Study Closure.\nEnsures that appropriate billing or charging mechanisms are in place for research charges related to research studies. Requires familiarity with research study budgets.\nPerforms research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.\nPartners and coordinates with regulatory compliance including preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety forms. Ensures that all study documents are complete and that records are retained per federal, state and institutional standards.\nObtains knowledge of departmental functions through in-service trainings with Physicians, attending workshops, seminars, or participating in investigator meetings when they occur.\nConducts and coordinates study-monitoring visits. Answer audits findings and quality assurance findings of assigned research studies to check the accuracy, integrity, and consistency of research studies.\nLearns how accurately complete pulmonary specific assessments including Pulmonary Function Testing, Six-Minute Walk Test, Standardized Questionnaires, etc. 
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KEY SUCCESS FACTORS

\n\nResearch certification or other certifications per specialty area preferred\nPhlebotomy and Lab skills preferred\nSpanish Speaking Skills beneficial but not essential  \nIndependence\nProven written and oral communication skills.\nFamiliarity and Proficiency with Microsoft Suite (Excel, Word, Teams, Outlook, SharePoint)\nAbility to Adapt to changes in assigned projects, tasks, and timelines\nAbility to manage time reactive projects in order to meet deadlines.\nExceptional ability to establish and maintain effective working relationships.\n\n

Belonging Statement

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We believe that all people should feel welcomed, valued and supported, and that our workforce should be reflective of the communities we serve.

QUALIFICATIONS

EDUCATION - Bachelor's or 4 years of work experience above the minimum qualificationEXPERIENCE - Less than 1 Year of Experience