On-Site Clinical Research Coordinator – Plano, TX

ACRC Trials; Plano (TX); On-site; USD 60,000 - 80,000; Full time

Job summary

ACRC Trials is seeking a Clinical Research Coordinator for a full-time, on-site role based in Plano, TX. You will coordinate all aspects of clinical trials, including participant recruitment, screening, enrollment, data capture, and regulatory compliance, ensuring proper documentation and safety reporting.

Hand-on experience with informed consent, study protocols, and collaboration with investigators and sponsors is essential.

Qualifications

• Demonstrated clinical research experience, ideally in studies involving human participants.
• Strong understanding of research methodologies and protocol management.
• Experience obtaining and documenting informed consent per regulatory guidelines.
• Knowledge of clinical trials operations, including scheduling visits and data collection.
• Healthcare or life sciences background and/or certification as a Clinical Research Coordinator is beneficial.
• Excellent organizational skills and ability to manage multiple studies.
• Effective written and verbal communication with participants, investigators, Sponsors.
• Familiarity with GCP, FDA regulations, and IRB processes preferred.
• On-site work in Plano, Frisco, and Carrollton, TX.

Responsibilities

• Coordinate all aspects of assigned clinical trials.
• Oversee participant recruitment, screening, and enrollment with initial assessments.
• Maintain source documents and update case report forms.
• Track study timelines and communicate with investigators, sponsors, and monitors.
• Support participant safety and report adverse events.
• Organize regulatory files and contribute to clinic operations and patient experience.

Skills

Clinical research experience

Regulatory/documentation

Communication skills

Organizational skills

Education

Healthcare or life sciences background

Clinical Research Coordinator certification (optional)

Job description

ACRC Trials is seeking a Clinical Research Coordinator for a full-time, on-site role based in Plano, TX. You will coordinate all aspects of clinical trials, including participant recruitment, screening, enrollment, data capture, and regulatory compliance, ensuring proper documentation and safety reporting.

Hand-on experience with informed consent, study protocols, and collaboration with investigators and sponsors is essential.