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UTHealth Houston · 1 day ago

Research Coordinator III - School of Public Health

Texas, United States

Full-time

Onsite

Senior Level

5+ years exp

UTHealth Houston is Texas’ resource for healthcare education, innovation, scientific discovery, and excellence in patient care. The Research Coordinator III will plan and coordinate project monitoring and evaluation tasks, including survey development, staff training, and dissemination of findings for a breast and cervical cancer early detection program aimed at underserved women.

EducationHealth CareProfessional Services

No H1B

Responsibilities

Supports in developing program outcomes Lead the design, development, and refinement of surveys to assess intervention process and behavioral outcome in accordance with the logic model and funding agency (CPRIT) reporting requirements and evaluation goals and entering all program forms into REDCap

Conduct literature reviews, evaluate, and recommend validated measures to determine appropriate constructs and instruments for inclusion in study surveys

Develop surveys and data dictionaries, plan survey skip logic, and lead instrument documentation to ensure methodological integrity and alignment with evaluation goals

Coordinate evaluation activities, including developing and managing participant recruitment workflows, survey protocols, consent procedures, developing baseline and follow-up participant tracking systems, and incentive tracking systems

Draft, maintain, and implement a manual of procedures (MOP) related to survey administration, process evaluation, and data quality workflows

Build, test, and oversee the HMH/SEMM survey REDCap database system used for survey data collection and HMH/SEMM implementation tracking system in REDCap used to monitor implementation of the intervention. Troubleshoot and provide training and re-training to improve data collection (surveys and intervention data collection). Monitor data collectors’ adherence to study protocols. Provide oversight of to personnel on data entry to, ensure consistency in data collection procedures

Assist the program manager in Provides day-to-day project management coordination for monitoring and evaluation activities including implementers’ adherence to data entry protocols and conducting training or re-training as needed to support the quality of documentation by implementers, REDCap tracking systems, observation activities, and data

Coordinate communication among evaluators, investigators, and implementation teams to ensure study tasks are completed on schedule

Maintain organized, confidential evaluation records and documentation required for reporting to funders and the IRB

Draft internal and external evaluation reports, including summaries of progress towards goals, participant follow-up completion, and data quality indicators, corresponding CPRIT requirements, and evaluation goals

Contribute to grant reporting, grant proposal preparation, conference abstracts, conference posters, and manuscripts prepared for publication

Perform other study-related responsibilities as assigned

Qualification

Survey DevelopmentREDCapProject ManagementClinical Research CertificationCommunication Skills

Required

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

Five (5) years of relevant experience. May substitute required experience with equivalent years of education beyond the minimum education requirement

Excellent communication skills both written and verbal

Working knowledge of MS Office

Depending on clinical trial, if nursing type duties are required, an RN license issued by the state of Texas is required

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

Employees must permanently reside and work in the State of Texas

Preferred

Certification from the Society of Clinical Research Associates (SOCRA), Association of Clinical Research Professionals (ACRP), Research Administrators Certification Council (RACC), Certified IRB Professional (CIP) or, Regulatory Affairs Certification (RAC)