Research Coordinator III - Children's Learning Institute CAE

UTHealth Houston•Houston, TX

14h•Onsite

About The Position

UTHealth Houston's Children's Learning Institute is hiring a Research Coordinator! The Research Coordinator III supports the Centralized Assessment Entity (CAE) by leading fidelity and monitoring activities to ensure consistent program implementation and compliance with established Texas Rising Star standards. This role is responsible for analyzing and interpreting program data to assess performance, identify trends, and highlight areas for continuous improvement. The Research Coordinator extracts, manages, and maintains data from multiple sources and translates findings into clear, actionable insights. Other responsibilities include developing data visualizations, dashboards, and reports to support decision-making, stakeholder communication, and statewide reporting requirements. In collaboration with internal teams and partners, the incumbent monitors program implementation, evaluates data quality, and provides recommendations to strengthen processes and improve overall program quality. This position requires strong analytical skills, attention to detail, and the ability to communicate complex data clearly and accessibly, along with knowledge of the Texas Rising Star program and its standards.

Requirements

Completion of Human Research Subjects training.
Demonstrated data management skills.
Excellent communication skills both written and verbal.
Detailed oriented.
Bachelor's Degree in a related field required.
5 years of relevant experience required.
Employees must permanently reside and work in the State of Texas.

Nice To Haves

Strong data analysis and problem-solving skills
Advanced proficiency in Microsoft Excel (e.g., data analysis, pivot tables, formulas)
Experience with data visualization tools (e.g., Power BI, Tableau, or similar)
Knowledge of Texas Rising Star standards and program requirements
High attention to detail and data accuracy
Ability to communicate findings clearly to both technical and non-technical audiences
Experience supporting program monitoring, evaluation, or quality improvement efforts
Master's Degree preferred
May substitute required education with equivalent years of experience beyond the minimum experience requirement.
May substitute required experience with equivalent years of education beyond the minimum education requirement.
Health Services\Certified Clinical Research Professional (CCRP) by Society of Clinical Research Associates (SOCRA) preferred

Responsibilities

Assists with human subjects research activities, including participant recruitment, informed consent, data collection through surveys, interviews, and observations, and ensuring that all activities are conducted according to study protocols.
Maintains confidential records of collected data, ensures accuracy, compliance and integrity of data. Data may include human subject data and departmental programmatic data. Supports Data Management Sharing (DMS) plan.
Finalizes annual progress reports and applications for various committees and ensures that all staff have received the proper training/attended the appropriate training courses.
Assists in the preparation of progress and annual reports, contracts and grant proposals to various funding agencies; works closely with the Office of Sponsored Projects on the submission of grants.
May assist with regulatory submissions (i.e. Institutional Review Board(s), FDA, etc).
Assists investigator with quantitative and qualitative data analysis, including statistical tests and the creation of figures, tables, and graphs. Helps prepare research papers, presentations, and reports including manuscripts for publications and conferences.
Prepares or assists in the preparation of budgets, initiates re-budgeting requests based on the needs of research staff, and authorizes expenditures for multiple projects. Attends research planning meetings to prepare budget drafts for departmental leadership approval. Reconcile and monitor invoices.
Responsible for coordinating and responding to site monitoring visits, audits, and inspections.
May be responsible for maintaining study materials (i.e. test kits, investigational drugs and devices).
May provide administrative direction training and guidance to study personnel within department.
May provide recommendations by identifying opportunities to enhance, re-terminate, or re-direct resources across various research projects to ensure timely completion of project guidelines.
Supports complex scheduling and logistical needs to meet projects' expectations.
Performs other duties as assigned.