Ophthalmology Clinical Research Coordinator II - Onsite

Baylor College of Medicine; Houston (TX); On-site; USD 47,000 - 56,000; Full time

Job summary

Baylor College of Medicine in Houston, TX seeks a Research Coordinator II in Ophthalmology to coordinate clinical studies, ensure protocol compliance, and manage participant interactions. The role requires collaboration with investigators, sponsors, and supporting services to achieve milestones, with emphasis on data integrity and participant safety.

The candidate will handle regulatory submissions, imaging coordination, data entry, and study document management while supporting IRB submissions

Qualifications

• Bachelor's degree in a related field; four years of related experience may substitute for degree requirement.
• One year of relevant experience.

Responsibilities

• Screens, recruits, enrolls, and consents research participants according to protocol requirements.
• Explains study procedures and educates participants regarding research study expectations and requirements.
• Schedules and coordinates study visits, laboratory testing, imaging procedures, and specialty evaluations.
• Coordinates participant follow-up visits and maintains participant retention throughout the study duration.
• Collects, processes, ships, and maintains documentation for blood and other biological specimens in accordance with protocol requirements.
• Enters and maintains study data in EDC systems, databases, and institutional systems.
• Maintains regulatory files, study binders, delegation logs, essential documents, and training records.
• Prepares and submits IRB applications, amendments, continuing reviews, reportable events, and study closure documentation.

Education

Bachelor's degree in a related field

Job description

Baylor College of Medicine in Houston, TX seeks a Research Coordinator II in Ophthalmology to coordinate clinical studies, ensure protocol compliance, and manage participant interactions. The role requires collaboration with investigators, sponsors, and supporting services to achieve milestones, with emphasis on data integrity and participant safety.

The candidate will handle regulatory submissions, imaging coordination, data entry, and study document management while supporting IRB submissions