Facility: Baylor Research Institute - Plano

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Department: Cardiology 

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Shift/Status:  Full Time 40 hours/week Monday - Friday

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Onsite, may require travel to McKinney/Denton.

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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 Supervisor oversees daily supervision of Clinical Research staff. This position develops, negotiates, and monitors budgets for funded research projects. It also facilitates the implementation of clinical research projects and ensures quality and timely completion.

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Essential Functions of the Role

\n\nWrites and assists in the development of proposals, grants, contracts, and budgets for the department.\nAssists in developing new protocols and materials from study sponsors. Provides input to Principal Investigators and management on clinical and research issues to establish financial and clinical feasibility.\nAssists various PIs, through delegated authority, in conducting clinical trials per federal, state, and institutional guidelines.\nPrepares initial project submissions, amendment notifications, SAE reports, continuing review reports, and other reports for the IRB. Reviews staff-prepared submissions to ensure they meet established standards.\nOversees case report form completion by staff for all studies. Assists in coordinating audits by study sponsor monitors. Monitors assigned Clinical Research funds.\nOrientates, trains, supervises, and evaluates Clinical Research staff. Encourages growth through complex responsibilities and education programs. Coordinates project assignments for staff.\nEstablishes and maintains good relations with the public, patients, and staff; promotes the department's research programs.\nMonitors communication with the IRB, Food and Drug Administration (FDA), and other applicable regulatory agencies.\n\n

Key Success Factors

\n\nResearch certification or other certifications per specialty area preferred.\nBasic Life Support (BLS) per department requirements.\nProven written and oral communication skills.\nProven computer skills, including Microsoft Office, Excel, and PowerPoint.\nAbility to manage time impressible projects in order to meet deadlines.\nAbility to establish and maintain effective working relationships.\nExcellent leadership skills.\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 - 2 Years of Experience