Clinical Research Coordinator I - Trials & Compliance

Clinical & Support Options Inc; Dallas (TX); On-site; USD 30,000 - 36,000; Full time

Job summary

Alliance Clinical Network is seeking a Clinical Research Coordinator I in Dallas, TX. This role supports clinical trials by coordinating visits, collecting data, and ensuring protocol compliance, with direct participant interaction and health monitoring.

You will document informed consent, manage regulatory files, and assist with monitoring visits while collaborating with the PI to maintain study integrity and GCP standards.

Qualifications

• Minimum of 2 years of experience with phlebotomy and EKG procedures and CPT license.
• Associate’s degree in healthcare or related field, or equivalent experience.
• Minimum 2 years of healthcare setting experience.
• Minimum 2 years of experience with FDA regulations and GCP.

Responsibilities

• Coordinate study visits and manage data collection per protocol.
• Obtain and document informed consent from participants.
• Maintain regulatory files and ensure GCP/compliance.
• Administer questionnaires and monitor participant adherence.
• Enter data into EDC systems and resolve data queries.
• Support recruitment and engagement of study participants as needed.
• Monitor IP dispensing and accountability and coordinate with labs.

Skills

Analytical thinking

Attention to detail

Communication skills

Customer service

Multitasking

Education

Associate's degree in healthcare or related field

Job description

Alliance Clinical Network is seeking a Clinical Research Coordinator I in Dallas, TX. This role supports clinical trials by coordinating visits, collecting data, and ensuring protocol compliance, with direct participant interaction and health monitoring.

You will document informed consent, manage regulatory files, and assist with monitoring visits while collaborating with the PI to maintain study integrity and GCP standards.