Clinical Research Coordinator

Job Description

Company Description

Quality Medical Research (QMR) conducts cutting-edge clinical trials across all phases, with a strong focus on gastroenterology. Our studies range from early-phase safety trials to large-scale, late-phase efficacy research. We partner with leading sponsors and investigators to bring innovative therapies to patients faster. QMR is now expanding into primary care research, broadening our mission to advance healthcare through clinical excellence, scientific integrity, and a compassionate, patient-first approach. We are committed to creating tailored treatment plans that focus on restoring wellness and managing symptoms in a comfortable and private office setting.

Role Description

This is a full-time, on-site role for a Clinical Research Coordinator located in Nashville, TN. The Clinical Research Coordinator will be responsible for managing clinical trials, ensuring adherence to protocols, obtaining informed consent from participants, and coordinating research activities. Additional responsibilities include maintaining compliance with regulations, facilitating communication with study stakeholders, and supporting the overall success of the clinical research program.

Qualifications

• Knowledge and experience with informed consent processes
• Phlebotomy and EKG experience
• Proficiency in managing research protocols and conducting studies
• Demonstrated Clinical Research Experience, including familiarity with clinical trials
• Strong organizational, communication, and teamwork skills
• Ability to work independently and manage multiple tasks effectively
• Certification as a Clinical Research Coordinator (CCRC) is a plus
• Associate degree in a clinical or scientific field required; Bachelor’s degree preferred.
• Minimum of 2 years’ experience as a Clinical Research Coordinator on pharmaceutical phase II or III trials (GI research experience preferred).