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Clinical Research Coordinator I, II, or III - Internal Medicine / Rheumatology - 250000JP
Clinical Research Coordinator I, II, or III - Internal Medicine / Rheumatology - 250000JP-March 2024
Houston
Mar 21, 2026
About Clinical Research Coordinator I, II, or III - Internal Medicine / Rheumatology - 250000JP

What we do here changes the world. UTHealth Houston is Texas' resource for healthcare education, innovation, scientific discovery, and excellence in patient care. That's where you come in.

The Division of Rheumatology seeks a Clinical Research Coordinator, Level I, II, or III. The ideal candidate will have experience as a clinical research coordinator for interventional studies, direct interaction with patients, experience with inclusion/exclusion criteria screening, data entry, query resolution, phlebotomy, sample processing, and federal policy regarding the protection of human subjects. All qualified candidates will be considered.

Once you join us you won't want to leave. It's because we reward our team for the excellent service they provide. Our total rewards package includes the benefits you'd expect from a top healthcare organization (benefits, insurance, etc.), plus:

100% paid medical premiums for our full-time employeesGenerous time off (holidays, preventative leave day, both vacation and sick time - all of which equates to around 37-38 days per year)The longer you stay, the more vacation you'll accrue!Longevity Pay (Monthly payments after two years of service)Build your future with our awesome retirement/pension plan!We take care of our employees! As a world-renowned institution, our employees' wellbeing is important to us. We offer work/life services such as...

Free financial and legal counselingFree mental health counseling servicesGym membership discounts and access to wellness programsOther employee discounts including entertainment, car rentals, cell phones, etc.Resources for child and elder carePlus many more!Position Summary:

The Division of Rheumatology seeks a Clinical Research Coordinator, Level I, II, or III. The ideal candidate will have experience as a clinical research coordinator for interventional studies, direct interaction with patients, experience with inclusion/exclusion criteria screening, data entry, query resolution, phlebotomy, sample processing, and federal policy regarding the protection of human subjects. All qualified candidates will be considered.

Assists with the day-to-day administrative project management and may provide scientific direction forresearch projects of considerable scope and complexity.

Position Key Accountabilities:

Assists with the day-to-day project management coordination for research projects to include personnel, facilities, and supplies supporting research project desired outcomes, budgets, and timeliness.Assists in preparing progress reports and grant proposals to private foundations and governmental agencies; works closely with the Office of Sponsored Projects on the submission of grants.Assists with the preparation/review of budgets, initiates re-budgeting requests based on the needs of research staff, and authorizes expenditures for multiple projects. Attend research-planning meetings to assist in preparing budget drafts for departmental leadership approval.Prepares annual progress reports and applications for various committees and ensures that all staff have received the proper training/attended the appropriate training courses.Maintains confidential records of collected data and ensures accuracy and integrity of data. Data may include patient data and departmental programmatic data.Prepares draft reports and communications for the departmental program/division leadership.Interacts with representatives from state, federal, and private agencies regarding proposals and funded projects.Provides work administrative direction and guidance to administrative staff personnel within department.May review contracts and develop training.Other duties as assigned.Certification/Skills:

Excellent communication skills both written and verbal.Working knowledge of MS Office.

Minimum Education:

Bachelor's degree in a related field or relevant experience in lieu of education.

Minimum Experience:

NonePhysical Requirements:

Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects.This position may include work involving potentially hazardous chemical, biological or radioactive agents.

Security Sensitive:

This job class may contain positions that are security sensitive and thereby subject to the provisions of Texas Education Code 51.215

Residency Requirement:

Employees must permanently reside and work in the State of Texas.

Equal Opportunity Employer - minorities/females/veterans/individuals with disabilities

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