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Location: Houston, TX
Contract: 6–12 months
Schedule: Up to 40 hours/week (based on patient enrollment)
We are seeking a Clinical Research Coordinator to support an upcoming HIV clinical trial focused on device and diagnostic testing. This hybrid role will require significant on-site presence in Houston, especially during participant enrollment and sample collection.
Coordinate day-to-day trial activities and patient visits
Ensure protocol compliance and accurate documentation
Support sample collection, device testing, and data entry
Liaise with clinical teams, labs, and external partners
Maintain regulatory and GCP standards
2+ years of clinical research experience, ideally in diagnostics or infectious disease
Strong organizational and communication skills
Experience with EDC systems and clinical documentation
Comfortable working on-site and engaging directly with participants