Clinical Research Coordinator II; Two Positions

ACRC Trials | DFW Area (Plano & Carrollton, TX)

Industry: Research Services

Employment Type:

Full-time

ACRC Trials is seeking an experienced and highly motivated Clinical Research Coordinator (CRC II) to join our growing team in the DFW area. With headquarters in Plano, TX and clinics across Austin, Plano, Carrollton, Frisco, and Grapevine, we are a leading clinical research organization known for high-quality trials and strong physician partnerships.

This is an excellent opportunity for an experienced coordinator who thrives in a fast-paced, patient-centered research environment and is confident working directly with physicians, sponsors, and study participants.

ACRC Trials is a premier clinical research organization dedicated to advancing medicine through high-quality, ethical, and patient-centered clinical trials. We partner with leading pharmaceutical companies, CROs, and physicians to deliver reliable data while providing an exceptional experience for study participants.

Our therapeutic expertise includes family medicine, dermatology, pediatrics, pediatric dermatology, and pulmonology, with a strong and well-established focus in vaccine clinical research. ACRC Trials is recognized for operational excellence, high enrollment performance, and a collaborative culture built on professionalism, integrity, and continuous growth.

• Coordinate and manage multiple clinical research protocols across various therapeutic areas
• Conduct subject screening, enrollment, and follow-up visits per protocol requirements
• Perform study visits, vital signs, ECGs, and specimen collection (phlebotomy experience a plus)
• Ensure accurate and timely source documentation and EDC entry
• Work with the regulatory team and as directed, help in coordination of reg documents, and ensure compliance with ICH-GCP, FDA regulations, and SOPs
• Communicate effectively with investigators, sponsors, CROs, monitors, and internal teams
• Support recruitment efforts and maintain strong patient relationships
• Prepare for and participate in monitoring visits, audits, and inspections
• Track and report adverse events and protocol deviations as required

• Prior clinical research industry experience is required
• Current certification through SOCRA (CCRP) or ACRP (CCRC) is a PLUS
• Strong background in medicine and clinical research operations
• Thorough knowledge of medical research processes and documentation
• Knowledge of ICH Guidelines, GCP, and FDA regulations
• Ability to manage multiple protocols simultaneously
• Excellent verbal and written communication skills
• Highly organized, detail-oriented, and dependable
• Outgoing, confident, and comfortable interacting with physicians and patients
• Strong recruiting and patient engagement skills
• Proficient with computers and EDC systems

• Vaccine clinical trial experience a strong plus
• Experience across multiple therapeutic areas

• Opportunity to work with a high-performing research team
• Exposure to a diverse portfolio of clinical trials and sponsors
• Supportive, professional, and growth-oriented environment

ACRC Trials is an equal opportunity employer and values professionalism, integrity, and collaboration in advancing clinical research.