Supv Clinical Research

Requisition: 26008816

Company: Baylor Scott & White Health

Location: Plano, Texas, United States

Employment type: full time

Category: Allied Health

Industry: Healthcare

Level: Manager

Shift: Day JobPosted: 2026-10-04

About Us: 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. Our Core Values are: We serve faithfully by doing what's right with a joyful heart. We never settle by constantly striving for better. We are in it together by supporting one another and those we serve. We make an impact by taking initiative and delivering exceptional experience.

Benefits: 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: Immediate eligibility for health and welfare benefits 401(k) savings plan with dollar-for-dollar match up to 5%Tuition ReimbursementPTO accrual beginning Day 1Note: Benefits may vary based upon position type and/or level.

Job Summary: 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. Essential Functions of the RoleWrites and assists in the development of proposals, grants, contracts, and budgets for the department. Assists 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. Assists various PIs, through delegated authority, in conducting clinical trials per federal, state, and institutional guidelines. Prepares 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. Oversees case report form completion by staff for all studies. Assists in coordinating audits by study sponsor monitors. Monitors assigned Clinical Research funds. Orientates, trains, supervises, and evaluates Clinical Research staff. Encourages growth through complex responsibilities and education programs. Coordinates project assignments for staff. Establishes and maintains good relations with the public, patients, and staff; promotes the department's research programs. Monitors communication with the IRB, Food and Drug Administration (FDA), and other applicable regulatory agencies.

Key Success Factors: Research certification or other certifications per specialty area preferred. Basic Life Support (BLS) per department requirements. Proven written and oral communication skills. Proven computer skills, including Microsoft Office, Excel, and PowerPoint. Ability to manage time impressible projects in order to meet deadlines. Ability to establish and maintain effective working relationships. Excellent leadership skills.

Belonging Statement: We believe that all people should feel welcomed, valued and supported.

QUALIFICATIONS: EDUCATION - Bachelor's or 4 years of work experience above the minimum qualificationEXPERIENCE - 2 Years of Experience