Senior Research Coordinator: IRB & Clinical Trials

UTHealth Houston; Houston (TX); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

100% paid medical premiums

Generous time off

Longevity pay

Job summary

UTHealth Houston’s Ophthalmology Department is seeking a Research Coordinator III to join their team. You will support human subjects research, IRB submissions, budgeting, data management, and coordination across multiple projects.

The role requires strong organizational skills, 4 years of research experience, and ability to train staff in IRB processes. You will partner with collaborators from Retina Consultants of Texas, Baylor, and Methodist Hospital to advance clinical studies.

Qualifications

• Bachelor's Degree in a related field is required; Master's Degree preferred.
• Minimum 4 years of relevant research experience.
• Experience with IRB processes and regulatory submissions is preferred.

Responsibilities

• Assists with human subjects research activities including participant recruitment and data collection.
• Maintains confidential data records ensuring integrity and compliance.
• Prepares budgets, reports and grant proposals; coordinates with funded projects.
• Provides regulatory support for IRB submissions and study protocols.
• Trains staff in IRB processes and submission preparation.

Skills

Excellent communication skills

Detailed oriented

Data management

Education

Bachelor's Degree in a related field

Master's Degree preferred

Job description

UTHealth Houston’s Ophthalmology Department is seeking a Research Coordinator III to join their team. You will support human subjects research, IRB submissions, budgeting, data management, and coordination across multiple projects.

The role requires strong organizational skills, 4 years of research experience, and ability to train staff in IRB processes. You will partner with collaborators from Retina Consultants of Texas, Baylor, and Methodist Hospital to advance clinical studies.