Clinical Research Coordinator II/III

Company Description

AARA Clinical Research is deeply rooted in the success of Arizona Arthritis & Rheumatology Associates (AARA), one of the largest rheumatology practices in the United States. With over 30 years of experience in clinical research, AARA Clinical Research has participated in more than 1,000 studies across various phases and therapeutic areas. The organization operates within a robust network of 25 private practice offices nationwide, supported by 150 dedicated research staff and 40 experienced Principal Investigators. AARA Clinical Research is committed to advancing medical science and improving patient care through high-quality clinical research.

Role Description

This is a full-time, on-site role located in Fort Worth, TX, as a Clinical Research Coordinator II/III. The Clinical Research Coordinator will be responsible for managing the operational aspects of clinical trials, which includes coordinating pharmaceutical drug inventory, executing clinical trial protocols, obtaining informed consent, particpant recruitment, overseeing study participants enrollment, and ensuring compliance with regulatory and ethical standards. Additional responsibilities involve maintaining accurate study documentation, collaborating with Principal Investigators, and ensuring the smooth execution of clinical trials from start to finish.

Qualifications

• Experience in Clinical Research, including Phase II-IV Clinical Trials
• Proficiency in phlebotomy, lab processing, and intake assessments (vital signs, medical history, etc.)
• Strong ability to manage implement, and adhere to Research Protocols in compliance with ethical standards and regulations (GCP & CFR)
• Knowledge of clinical research regulations and experience collaborating with investigative teams
• Strong organizational, time management, and problem-solving skills
• Excellent communication skills and the ability to work effectively in a fast-paced, team-oriented environment
• Bachelor’s degree in a health or science-related field preferred
• Certification as a Clinical Research Professional (such as ACRP or SOCRA) is a plus