- HonorHealth Scottsdale Thompson Peak Medical Center
- Deer Valley, AZ
- Full-Time
- 13 days ago
Analyst II - Clinical Trials Operations.
Before you go
Before you leave us, sign up for our email alerts
We don't do job spam, just the best digital jobs delivered straight to your inbox.
Analyst II - Clinical Trials Operations: our view in 3 lines...
- The Role:This role supports clinical trial operations in a healthcare system by managing studies through start-up and activation.
- The Person:The person will oversee assigned clinical trials, build and review study records in CTMS and EMR systems, track timelines and barriers, prepare status updates for leadership, and help resolve operational issues.
- Requirements:The role requires experience in Clinical Research Operations, CTMS/EMR builds, study start-up, research business operations, quality reviews, and a certification in clinical research such as ACRP-CP, CCRC, or CCRP.
About the role
Primary City/State:
Deer Valley - 2502 W Utopia Rd Phoenix, AZ 85027
Category:
Research Operations
Shift:
Day
Department:
HRI-Business Services ABC&E


Hybrid
Must reside in Arizona


Great care starts with great people. (Like you.)
At HonorHealth, you’ll find something special. From humble beginnings in 1927 to one of Arizona’s largest nonprofit healthcare systems, our culture is built on warmth and neighborly kindness. Behind every smile is a highly skilled professional with deep expertise and an unwavering dedication to what matters most — caring for the health and well-being of people and communities across the greater Phoenix area.
Responsibilities:


- Portfolio Management
Independently oversee assigned clinical trials through start-up and activation.
Ensure accuracy, compliance, and timely completion of deliverables. - Build & Review Study Records
Create and maintain CTMS and EMR study builds with minimal oversight
Perform detailed quality reviews to identify and resolve discrepancies - Own Study Progress & Reporting
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 - Mentor & Collaborate
Support training of junior staff through knowledge sharing.
Partner with investigators and stakeholders to resolve operational issues. - Performs other duties as assigned.
- High School Diploma or 4 years of relevant experience Required or
- Associates or 2 years of relevant experience Required
- Bachelors in Healthcare, Science, Business, or related discipline Preferred
- , Experience in Clinical Research Operations, with demonstrated competency in CTMS/EMR builds, study start-up, or research business operations 2 years Required
- , 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


We're all in for your career.

