Research Coordinator I - Internal Medicine, Critical Care (Bilingual

Research Coordinator I

We are hiring a Research Coordinator I (Full-time) to join the UTHealth Houston McGovern Medical School Department of Internal Medicine, Critical Care in Houston, Texas. In this role, you will coordinate the day-to-day operations of multiple inpatient and outpatient clinical research studies, including participant screening, recruitment, informed consent, study visits, regulatory documentation, data collection, and sponsor communications. This position works closely with physicians, research staff, and study sponsors to ensure studies are conducted in compliance with GCP, FDA regulations, and institutional policies.

Bilingual in Spanish, strongly preferred, along with knowledge of Good Clinical Practice (GCP), HIPAA, FDA regulations, and IRB processes also preferred.

Assists with human subject research project conduct and management, including participant recruitment and data collection, entry, management, and analysis. Assists with research project logistics, maintaining records, preparing reports, and meeting research milestones and deadlines.

The Research Coordinator I, will support the Division of Pulmonary, Critical Care & Sleep Medicine at UTHealth Houston. Our research portfolio includes industry-sponsored, investigator-initiated, observational, registry, and device clinical trials focused on pulmonary diseases, critical care, sleep medicine, pulmonary hypertension, COPD, asthma, interstitial lung disease, and other respiratory conditions. The coordinator will collaborate with multiple principal investigators, physicians, research coordinators, nurses, regulatory staff, and sponsors to conduct high-quality clinical research while ensuring participant safety and regulatory compliance.

Under supervision, assists with human subjects research activities, including participant recruitment, informed consent, data collection through surveys, interviews, observations, and ensuring that all activities are conducted according to study protocols.

Organizes, cleans, and maintains databases to ensure accurate data entry and preparation for analysis under close supervision.

Maintains confidential records of collected data and ensures accuracy, compliance, and integrity of data. Data may include human subject data and departmental programmatic data. Supports Data Management Sharing (DMS) plan.

Prepares 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 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).

Assist investigator with quantitative and qualitative data analysis, including the creation of figures, tables, and graphs. Helps prepare research papers, presentations, and reports including academic publications and conferences.

Conduct reviews of academic journals and databases to gather relevant articles and publications as directed to help prepare manuscripts for publication.

Assists with the preparation of budgets and reviews re-budgeting needs and expenditures. Attends research-planning meetings to assist in preparing budget drafts for departmental leadership approval. Assists with invoicing.

Assists in preparing for and responding to site monitoring visits, audits, and inspections.

May be responsible for maintaining study materials (i.e. test kits, investigational drugs and devices).

Performs other duties as assigned.

Bilingual in Spanish, strongly preferred.

Knowledge of Good Clinical Practice (GCP), HIPAA, FDA regulations, and IRB processes, preferred.

Must be detail-oriented and able to work independently while collaborating within a multidisciplinary team.

Bachelor's Degree in a related field required May substitute required education with equivalent years of experience beyond the minimum experience requirement.

None

Exerts up to 20 pounds of force occasionally and/or up to 10 pounds frequently and/or a negligible amount constantly to move objects.

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