Research Coordinator III - Pediatrics - CRA Neurology Research
Listed on 2026-10-15
-
Research/Development
Clinical Research
Research Coordinator III
- Pediatrics - CRA Neurology Research
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Job Title:
Research Coordinator III
- Pediatrics - CRA Neurology Research Division: TCH Departments Work Arrangement:
Hybrid
Location:
Houston, TX Salary Range: $57,320 - $67,435 FLSA Status:
Exempt
Work Schedule:
Monday – Friday, 8 a.m. – 5 p.m. Summary
The Research Coordinator III independently manages the day-to-day operations of clinical research studies conducted through the Center for Research Advancement (CRA), supporting the Neurology Division within the Department of Pediatrics. Responsibilities include participant screening and enrollment, study coordination and monitoring, collection and management of research data, and communication with investigators, sponsors, and study participants.
The position is accountable for ensuring the accuracy, integrity, organization, and safety of study-related data and research participants while maintaining compliance with protocol, regulatory, and institutional requirements.
This role collaborates closely with Principal Investigators, physicians, and multidisciplinary research teams to implement clinical trial protocols, coordinate study activities, and support ongoing participant follow-up.
The position requires strong knowledge of FDA regulations, Good Clinical Practice (GCP) guidelines, human subjects research protections, and the ability to interpret and apply complex clinical research protocols and study requirements.
Operating independently with minimal supervision, the Research Coordinator III manages significant components of large and complex clinical trials or assumes full responsibility for one or more smaller clinical research studies.
The role requires advanced proficiency across all core clinical research coordination functions, including participant recruitment and consenting, protocol implementation, regulatory compliance, investigational product accountability, data management, and study documentation. Success in this position requires sound judgment, attention to detail, and the ability to ensure protocol adherence, data integrity, participant safety, and timely study execution.
Applicants must be willing to work in a fast pace setting, comfortable working in a team environment, and possess excellent communication skills. Position supports multiple complex studies in Pediatrics Neurology Research.
Occasional work on the weekends and after hours may be required.
Job DutiesClinically and administratively manages multiple complex clinical research studies, including high-volume and rapidly growing studies. Participates in study startup, qualification, and feasibility assessments and provides recommendations to Principal Investigators (PIs) and Research Managers regarding study implementation and operational needs.
Subject Visits – 30%
- Provides protocol-specific education and guidance to research participants within scope of practice.
- Reviews protocols with participants and verifies informed consent documentation before study activities.
- Coordinates protocol-required procedures, laboratory assessments, and study visits.
- Dispenses investigational products and maintains required drug accountability, inventory, and shipment records.
- Collects, processes, stores, and ships biological specimens according to protocols, laboratory procedures, and IATA requirements.
Screening & Enrollment – 20%
- Screens, recruits, and enrolls research participants according to approved protocols and regulatory requirements.
- Interviews participants and evaluates eligibility based on inclusion and exclusion criteria.
- Educates participants regarding study objectives, procedures, risks, benefits, and requirements.
- Facilitates and…
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