Clinical Research Coordinator

Job Description

About the Role and ACRC TRIALS

ACRC TRIALS is seeking an experienced Clinical Research Coordinator II to join our growing team across multiple locations (Plano, Frisco, Carrollton, TX) in the Dallas–Fort Worth metroplex. We are a leading clinical research organization dedicated to advancing medicine through innovative, patient-centered trials.

The ideal candidate is dependable, outgoing, and highly motivated, with strong organizational skills and the ability to manage multiple protocols across therapeutic areas. This role requires confidence in working with physicians, excellent patient interaction skills, and a commitment to accuracy and regulatory compliance.

ACRC TRIALS is recognized as one of the top research sites in the nation. With headquarters in Plano, TX, and sites in Austin, Carrollton, Plano, and Grapevine, we are committed to advancing medicine while delivering compassionate, high-quality care to our patients.

Key Responsibilities

• Coordinate and manage all aspects of clinical research studies from initiation to closeout.
• Recruit, screen, and consent study participants while maintaining high standards of patient care and confidentiality.
• Serve as the primary point of contact for physicians, patients, sponsors, and CROs.
• Ensure compliance with study protocols, GCP, ICH guidelines, FDA regulations, and internal SOPs.
• Collect, document, and maintain study data with accuracy and timeliness.
• Oversee investigational product accountability and study supply management.
• Conduct and document study visits, including vital signs, EKGs, blood draws, and other protocol-specific procedures.
• Prepare for and participate in sponsor / CRO monitoring visits, audits, and inspections.
• Support patient retention and engagement throughout trial participation.

Qualifications

Preferred Quailfications