Clinical Research Coordinator: Trials & Compliance

Haracec Complete Healthcare PLLC; El Paso (TX); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

401(k)

401(k) matching

Company car

Competitive salary

Dental insurance

Health insurance

Paid time off

Training & development

Vision insurance

Job summary

Haracec Complete Healthcare PLLC is seeking a Clinical Research Coordinator to manage clinical trials at the clinic, ensuring adherence to GCP, FDA regulations, and study protocols while maintaining data integrity and patient care.

The role coordinates day-to-day trial activities, screens and enrolls participants, documents consent, schedules visits, collects data, and liaises with investigators, sponsors, and site staff to support compliant, high-quality research outcomes.

Qualifications

• Degree in health sciences, nursing, biology, or a related field preferred.
• Minimum of 1–2 years of clinical research experience preferred.
• Knowledge of GCP, FDA regulations, and clinical trial processes.
• Strong organizational, time-management, and documentation skills.
• Excellent communication and interpersonal abilities.
• Proficiency with electronic medical records and clinical trial databases.

Responsibilities

• Coordinate and manage assigned clinical trials from study start-up through close-out.
• Screen, recruit, and enroll eligible study participants according to protocol criteria.
• Obtain and document informed consent in compliance with regulatory requirements.
• Schedule and conduct study visits, assessments, and procedures per protocol.
• Collect, review, and enter study data accurately and timely into electronic data capture systems.
• Maintain regulatory binders and essential study documentation.
• Ensure compliance with GCP, FDA regulations, sponsor requirements, and clinic policies.
• Prepare for and participate in monitoring visits, audits, and inspections.
• Serve as a primary point of contact for sponsors, monitors, investigators, and site staff.
• Report adverse events, protocol deviations, and safety information as required.
• Assist with study feasibility assessments and start-up activities.
• Maintain confidentiality of patient and study information at all times.

Skills

GCP knowledge

Regulatory compliance

Communication skills

Documentation

Education

Health sciences degree

Tools

EMR systems

Clinical trial databases

Job description

Haracec Complete Healthcare PLLC is seeking a Clinical Research Coordinator to manage clinical trials at the clinic, ensuring adherence to GCP, FDA regulations, and study protocols while maintaining data integrity and patient care.

The role coordinates day-to-day trial activities, screens and enrolls participants, documents consent, schedules visits, collects data, and liaises with investigators, sponsors, and site staff to support compliant, high-quality research outcomes.