Clinical Research Coordinator I - Trial Coordination & Data

Houston Methodist; Houston (TX); On-site; USD 52,000 - 68,000; Full time

Job summary

Houston Methodist is seeking a Research Coordinator to manage day-to-day activities of research protocols, assess patient eligibility, and ensure accurate data collection and documentation.

The role requires collaboration with clinicians and staff, adherence to ICH/GCP guidelines, and reliable communication to support compliant, efficient clinical studies. Strong attention to detail and organizational skills are essential to maintain study quality and participant safety.

Qualifications

• Bachelor's degree required.
• Two years of research experience required.
• Ability to handle data and regulatory documentation.

Responsibilities

• Under the direction of senior staff, screens and interviews to evaluate patient eligibility.
• Coordinates data collection, documentation, and entry in source documents and CRFs.
• Schedules participant visits and manages study-related appointments and communications.
• Maintains study records and regulatory documentation in compliance with protocol and GCP.

Skills

Attention to detail

Communication skills

Data entry

Regulatory knowledge

Team collaboration

Education

Bachelor’s degree

Job description

Houston Methodist is seeking a Research Coordinator to manage day-to-day activities of research protocols, assess patient eligibility, and ensure accurate data collection and documentation.

The role requires collaboration with clinicians and staff, adherence to ICH/GCP guidelines, and reliable communication to support compliant, efficient clinical studies. Strong attention to detail and organizational skills are essential to maintain study quality and participant safety.