[Hiring] Imaging Research Associate I @Clario

Role Description

Clario, part of Thermo Fisher Scientific, is seeking an Imaging Research Associate I to support the coordination of site and operational activities across the full lifecycle of clinical imaging studies. In this role, you will work closely with project teams, sites, and sponsors to ensure the timely delivery of high‑quality study data and service deliverables. This position plays an important role in supporting compliant, efficient clinical research operations that help bring life‑changing therapies to patients faster.

Qualifications

• High school diploma or Associate/Bachelor’s degree in bioscience, computer science, information technology, or related field preferred
• Familiarity with PC-based computers and standard software packages (Word, Excel, email, databases)
• Knowledge of clinical trials process and good clinical practices preferred
• Ability to navigate networks and manage files effectively
• Strong attention to detail and organizational skills
• Excellent verbal and written communication skills
• Ability to work independently and in a team environment with changing priorities
• Professional, positive attitude and strong interpersonal skills
• Leadership qualities and ability to meet aggressive deadlines

Requirements

• Coordinate site and operational activities throughout the study lifecycle
• Assist in preparation and reproduction of study materials during start-up phase
• Follow up on outstanding documentation to complete site qualification
• Schedule logistical and technical trainings with site personnel
• Create test run requests for sites submitting digital data
• Review, process, track, and monitor all study-related data received from sites
• Assist in monitoring and resolving data discrepancies from clinical data management
• Manage site communications, generate reports and queries, and verify accuracy before distribution
• Investigate and complete logistical edit checks
• Report issues found with study systems (e.g., study database, reading analysis system)
• Perform day-to-day IQC activities including coordinating, requesting, tracking, and processing IQC data
• Ensure IQC data is collected and maintained according to SOPs and study protocol requirements
• Communicate with clinical study teams and sponsors regarding deliverables
• Maintain study database and prepare BMD Scan Review Forms
• Support Project Managers with project administration, tracking, and reporting
• Participate in project meetings, conference calls, and training sessions

Benefits

• Competitive compensation
• Private health insurance
• Engaging employee programs
• Flexible work schedules
• Attractive PTO plan
• Flex workspace