Clinical Research Coordinator Jobs in Houston, TX

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for managing and coordinating clinical trials and research studies under the supervision of a Principal Investigator (PI). This role ensures compliance with regulatory requirements, ethical standards, and study protocols while maintaining high-quality data collection and participant care.

Key Responsibilities:

Study Coordination:

• Oversee day-to-day operations of clinical trials.
• Ensure adherence to study protocols, Good Clinical Practice (GCP), and regulatory guidelines.
• Schedule and conduct participant visits, interviews, and follow-ups.
• Supervise research staff and volunteers, providing guidance and training to maintain high standards of study conduct.

Data Management:

• Collect, code, and enter research data into databases.
• Maintain accurate and complete study documentation, including case report forms and consent forms.
• Monitor data quality and resolve discrepancies.

Regulatory Compliance:

• Prepare and submit IRB documentation and amendments.
• Report adverse events and serious adverse events according to protocol, sponsor, IRB, and regulatory requirements.
• Ensure all study activities comply with FDA, OHRP, and institutional policies.
• Assist in audits and monitoring visits.

Participant Engagement:

• Recruit, screen, and enroll eligible participants.
• Educate participants on study procedures, risks, and benefits.
• Monitor participant safety and report adverse events.

Collaboration & Communication:

• Liaise with sponsors, CROs, labs, and other stakeholders.
• Coordinate with internal departments for study logistics.
• Provide regular updates to the PI and research team.
• Identify workflow improvements that enhance recruitment, enrollment, and study efficiency.

Qualifications & Skills:

• 2-3 years of clinical research coordination experience.
• Bachelor’s degree in a healthcare related field.
• Certification in clinical research (e.g., ACRP or SOCRA)
• GCP and/or IATA Certification
• Strong understanding of clinical trial processes and regulatory frameworks.
• Excellent organizational, communication, and interpersonal skills.
• Proficiency in electronic data capture systems and Microsoft Office Suite.
• Experience in nephrology, chronic kidney disease (CKD), dialysis, vascular access, or related therapeutic areas.

Work Environment:

• Typically based in Ambulatory Surgical Centers and Nephrology private research organizations.
• May require occasional travel for multi-site studies.
• Flexible hours depending on study demands.
• Growing research program with opportunities for professional development and advancement.

Pay: $20.00 - $30.00 per hour

Education:

• Bachelor's (Preferred)

Experience:

• Clinical research: 2 years (Required)

Language:

• Spanish (Preferred)

License/Certification:

• IATA Certification (Preferred)

Willingness to travel:

• 25% (Preferred)

Work Location: In person