Clinical Research Coordinator II - Drive Trials & Impact

BORAKA; Houston (TX); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Paid medical premiums for full-time

Generous time off

Longevity pay

Retirement pension plan

Financial counseling

Mental health counseling

Wellness program discounts

Employee discounts

Child and elder care resources

Job summary

UTHealth Houston is seeking a Clinical Research Coordinator to support human subjects research across the TMC and nationwide sites. You will help with recruitment, consent, data collection, and regulatory compliance in a multidisciplinary setting.

Responsibilities include protocol implementation, data entry in electronic capture systems, and collaboration with investigators, clinical staff, and sponsors. Some travel may be required; bilingual abilities are a plus.

Qualifications

• Bachelor's degree required; substitution with equivalent experience allowed.
• 2 years of relevant experience required; substitution with education possible.
• Experience with IRB submissions preferred.
• Familiarity with REDCap, EPIC, and MS Office platforms preferred.

Responsibilities

• Assist with human subjects research activities, including recruitment, consent, data collection and entry.
• Maintain confidential data records; ensure data integrity and compliance.
• Prepare progress reports and assist in contracting and grant submissions.
• Support regulatory submissions (IRB, FDA) as needed.
• Assist with data analysis, figures, and manuscript preparation.
• Coordinate budgets and attend planning meetings for budget drafting.

Education

Bachelor's degree in a related field

CITI training completion

Tools

REDCap

EPIC

Microsoft Office

Job description

UTHealth Houston is seeking a Clinical Research Coordinator to support human subjects research across the TMC and nationwide sites. You will help with recruitment, consent, data collection, and regulatory compliance in a multidisciplinary setting.

Responsibilities include protocol implementation, data entry in electronic capture systems, and collaboration with investigators, clinical staff, and sponsors. Some travel may be required; bilingual abilities are a plus.