Clinical Research Coordinator II: Study Enrollment & Ops

Dm Clinical Research Group; Irving (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

DM Clinical Research Group seeks a Clinical Research Coordinator II in Frisco, TX to ensure compliant, high-quality research at investigative sites and deliver top data quality to the sponsor. The role requires training, visits, data handling, and communication with sponsors, CROs, investigators, and patients.

The candidate will perform ALCOA-C compliant documentation, support enrollment targets, and uphold regulatory standards and study procedures across assigned protocols.

Qualifications

• High School Diploma or equivalent required; Bachelor's degree preferred.
• At least 2 years of CRC experience, preferably coordinating industry-sponsored vaccines.
• Proficient communication in English; bilingual English/Spanish preferred.

Responsibilities

• Conduct study subject visits and document procedures per protocol.
• Maintain ALCOA-C standards in all trial documentation.
• Perform data entry and resolve queries in a timely manner.
• Support enrollment goals and sponsor/CRO communications.
• Coordinate training and adherence to FDA, ICH-GCP guidelines.
• Ensure patient privacy and professional conduct at all times.

Skills

Detail-oriented

Multi-tasking

Proficient communication

Bilingual EN/ES preferred

Education

High School Diploma or equivalent

Bachelor's degree preferred

Foreign Medical Graduates preferred

Tools

EDC

IVRS

Job description

DM Clinical Research Group seeks a Clinical Research Coordinator II in Frisco, TX to ensure compliant, high-quality research at investigative sites and deliver top data quality to the sponsor. The role requires training, visits, data handling, and communication with sponsors, CROs, investigators, and patients.

The candidate will perform ALCOA-C compliant documentation, support enrollment targets, and uphold regulatory standards and study procedures across assigned protocols.