Clinical Research Nurse (Unblinded experience preferred)

ACRC Trials is seeking an experienced CRC (RN preferred) to join our growing research network across the DFW area. This role is ideal for someone who thrives in a fast-paced, patient-focused environment and has strong experience with investigational product (IP) handling and study execution.

• Serve as the unblinded managing IP preparation, storage, administration, and accountability
• Serve as blinded team member for treatment studies, as needed
• Maintain strict blinding integrity and prevent accidental unblinding
• Perform clinical procedures including injections, vitals, ECGs, and specimen collection
• Ensure accurate source documentation and EDC entry
• Support monitoring visits, audits, and regulatory compliance (GCP/FDA)
• Track and report AEs/SAEs and protocol deviations
• Assist with blinded CRC responsibilities as needed, including patient visits and study coordination

• RN preferred (strong unblinded CRC experience considered)
• Clinical research experience required; IP handling experience strongly preferred
• Knowledge of ICH-GCP and FDA regulations
• Detail-oriented, organized, and able to manage multiple studies

Join a high-performing team known for strong enrollment, quality data, and excellent sponsor relationships. conducting clinical trials with a team of award-winning physicians. Recognized for excellence by D Magazine's "Best Doctors," ACRC provides high-quality, accessible healthcare within its facilities. The organization is committed to advancing medical knowledge and introducing improved medications through pharmaceutical-sponsored research. ACRC emphasizes patient safety, ethical practices, and comprehensive medical evaluations to ensure the best care for clinical trial participants.

Role Description

This is a full-time, on-site role based in Plano, TX, for a Clinical Research Nurse. The primary responsibilities include managing clinical trials, ensuring compliance with research protocols, monitoring patient care, and maintaining detailed and accurate medical records. The Clinical Research Nurse will work collaboratively with physicians, sponsors, and other team members, focusing on patient safety and data integrity. Previous experience with unblinding processes is preferred.

Qualifications

• Proficiency in Nursing and general Nursing practices
• Strong foundation in Medicine, including administration of treatments and patient care
• Experience in Research, with the ability to implement and adhere to study Protocol standards
• Exceptional organizational and communication skills to work collaboratively in a team and with study participants
• RN license or equivalent nursing qualification in the state of Texas (required)
• Experience in clinical research or prior unblinded study experience is highly preferred
• CERTIFICATIONS: Clinical Research Certifications (such as ACRP or SOCRA) are a PLUS
• Pediatric experience a PLUS