Clinical Research Coordinator

Clinical Research Coordinator Pearland Neurology Services, PLLC Houston, TX Job Details Part-time | Full-time $20 - $32 an hour 6 hours ago Benefits Health insurance Dental insurance Paid time off Vision insurance Flexible schedule Qualifications Teamwork Master's degree Schedule management Bachelor's degree

Health Science Full Job Description 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.

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. 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.

Qualifications & Skills:

Bachelor's degree in health sciences, life sciences, or related field (Master's preferred). Certification in clinical research (e.g., ACRP or SOCRA) is a plus. 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.

Work Environment:

Typically based in hospitals, academic research centers, or private research organizations. May require occasional travel for multi-site studies. Flexible hours depending on study demands.

Job Types:

Full-time, Part-time Pay:

$20.00 - $32.00 per hour

Benefits:

Dental insurance Flexible schedule Health insurance Paid time off Vision insurance

Work Location:

In person