Clinical Trials Operations Analyst II

HonorHealth • Phoenix, AZ

1d

About The Position

Looking to be part of something more meaningful? At HonorHealth, you’ll be part of a team, creating a multi-dimensional care experience for our patients. You’ll have opportunities to make a difference. From our Ambassador Movement to our robust training and development programs, you can select where and how you want to make an impact. HonorHealth offers a diverse benefits portfolio for our full-time and part-time team members designed to help you and your family live your best lives. Visit honorhealth.com/benefits to learn more. Join us. Let’s go beyond expectations and transform healthcare together. HonorHealth is one of Arizona’s largest nonprofit healthcare systems, serving a population of five million people in the greater Phoenix metropolitan area. The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer care network, outpatient surgery centers, clinical research, medical education, a foundation, an accountable care organization, community services and more. With nearly 17,000 team members, 3,700 affiliated providers and close to 2,000 volunteers dedicated to providing high quality care, HonorHealth strives to go beyond the expectations of a traditional healthcare system to improve the health and well-being of communities across Arizona. Learn more at HonorHealth.com.

Requirements

• High School Diploma or 4 years of relevant experience Required or
• Associates or 2 years of relevant experience Required
• Experience in Clinical Research Operations, with demonstrated competency in CTMS/EMR builds, study start-up, or research business operations 2 years Required

Nice To Haves

• Bachelors in Healthcare, Science, Business, or related discipline Preferred
• Experience independently managing study start-up activities, conducting quality reviews, and preparing status reports for leadership Preferred
• Certification in clinical research (e.g., ACRP-CP, CCRC, CCRP) Preferred

Responsibilities

• Independently oversee assigned clinical trials through start-up and activation.
• Ensure accuracy, compliance, and timely completion of deliverables.
• Create and maintain CTMS and EMR study builds with minimal oversight
• Perform detailed quality reviews to identify and resolve discrepancies
• Serve as primary owner of assigned studies within the CTBO workflow.
• Provide regular updates on timelines, barriers, and progress.
• Prepare and deliver study status presentations for leadership
• Support training of junior staff through knowledge sharing.
• Partner with investigators and stakeholders to resolve operational issues.
• Performs other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees