Lead Pediatric Clinical Trials Coordinator

Baylor College of Medicine; Houston (TX); On-site; USD 71,000 - 83,000; Full time

Job summary

The Senior Research Coordinator at Baylor College of Medicine, Pediatrics Division, manages multiple high-volume clinical studies, ensuring compliant enrollment, screening and data collection. The role works closely with physicians and investigators, requiring deep knowledge of GCP and regulatory requirements, and strong data/documentation skills.

Onsite in Houston, TX, with standard weekday hours. Candidates should have extensive clinical research experience and the ability to independently

Qualifications

• Bachelor's degree in a Basic Science or related field; four years of related experience may substitute for degree requirement.
• Five years of relevant clinical research experience.
• Ability to work independently with minimal supervision.

Responsibilities

• Manage multiple studies in a high-volume, complex clinical trial setting.
• Lead feasibility reviews by evaluating protocol logistics, staffing, patient population and resources.
• Screening and enrollment of participants, including consent where applicable.
• Oversee subject visits, protocol education, and informed consent documentation.
• Collect and enter study data; ensure accurate documentation and data integrity in CTMS.
• Coordinate with investigators, physicians, nurses and data managers to support patient care and data capture.
• Adhere to FDA Good Clinical Practices and Baylor College of Medicine SOPs; prepare documentation for approvals and renewals.
• Communicate with sponsors and study sites; report adverse events as required.

Skills

Five years of relevant experience

Strong data management

Independent work capability

Education

Bachelor's degree in a Basic Science or related field

Associate's degree or higher

Tools

REDCap

Epic

CTMS

Microsoft Excel

Job description

The Senior Research Coordinator at Baylor College of Medicine, Pediatrics Division, manages multiple high-volume clinical studies, ensuring compliant enrollment, screening and data collection. The role works closely with physicians and investigators, requiring deep knowledge of GCP and regulatory requirements, and strong data/documentation skills.

Onsite in Houston, TX, with standard weekday hours. Candidates should have extensive clinical research experience and the ability to independently