Clinical Research Coordinator

CommonSpirit Health • Phoenix, AZ

7d • Onsite

About The Position

As our Clinical Research Professional, you will be instrumental in advancing medical knowledge by expertly managing and executing clinical trials. You will ensure the highest standards of data integrity, patient safety, and regulatory compliance throughout the research process. Every day you will manage trial activities, including participant recruitment, data collection, and documentation, serving as a key liaison for all stakeholders. You will ensure strict adherence to protocols and regulatory requirements from study initiation to completion. To be successful in this role, you will bring relevant clinical research experience and a strong understanding of regulatory guidelines. Your exceptional organizational skills, attention to detail, and ability to communicate effectively will be crucial in this dynamic field.

Requirements

• Bachelors Degree in a related field
• Three years clinical research experience

Responsibilities

• Coordinate and implement procedures to collect data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
• Coordinate patient care within the multi-disciplinary team.
• Act as a specialists/resource person; provide support, recommendations and advice to all personnel involved with the study.
• Able to review minimally necessary data extracts for the purpose of identifying potential research candidates from our patient population.
• If a potential candidate is identified, they will work with the Primary Physician to begin the consenting process.
• Participate in various study procedures that may include obtaining blood, tissue or other specimens for laboratory analysis; EKG, echocardiogram, exercise treadmill testing, monitoring devices; and/or cardiac catheterization and interventional procedures.
• Ensure compliance with protocol guidelines and requirements of the institutional review board (IRB) and FDA regulations.
• Responsible for preparation of IRB documents, including submission of clinical trial protocols, amendments and study modifications; reporting of serious adverse events; annual reports; and/or study closure.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level