Senior Clinical Research Coordinator, Pediatric Trials

Baylor College of Medicine; Houston (TX); Vor Ort; USD 70.000 - 95.000; Vollzeit

Zusammenfassung

Baylor College of Medicine in Houston, TX seeks a Senior Research Coordinator to manage and oversee complex pediatric clinical trials within the Department of Pediatrics. You will handle enrollment, screening, drug dispensation per protocol, data collection, and safety reporting under FDA GCP guidelines.

Independent day-to-day operation and data integrity are essential. With strong regulatory knowledge and experience in CTMS, REDCap, Epic systems, and Excel, you will collaborate with clinicians,

Qualifikationen

• Bachelor's degree in a Basic Science or related field required; four years of related experience may substitute for degree.
• Five years of relevant experience preferred; strong clinical research background is essential.
• Experience in interventional clinical trials and regulatory compliance highly desirable.

Aufgaben

• Manage multiple studies in pediatrics clinical trials with regulatory compliance.
• Lead feasibility reviews including protocol logistics, staffing and resources.
• Oversee enrollment, screening, and informed consent processes with participants.
• Coordinate subject visits, education, and protocol adherence across teams.
• Collect, enter, and verify data; manage CTMS and safety reporting to sponsors.
• Prepare documentation for protocol approvals and regulatory submissions.

Kenntnisse

Interventional clinical trials

Independent work

Communication

Problem solving

Data management

Ausbildung

Bachelor's degree in Basic Science or related field

Associate's degree or higher preferred

Tools

REDCap

Epic

CTMS

Microsoft Excel

Jobbeschreibung

Baylor College of Medicine in Houston, TX seeks a Senior Research Coordinator to manage and oversee complex pediatric clinical trials within the Department of Pediatrics. You will handle enrollment, screening, drug dispensation per protocol, data collection, and safety reporting under FDA GCP guidelines.

Independent day-to-day operation and data integrity are essential. With strong regulatory knowledge and experience in CTMS, REDCap, Epic systems, and Excel, you will collaborate with clinicians,