Clario
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.
What We Offer
Competitive compensation
Private health insurance
Engaging employee programs
Flexible work schedules
Attractive PTO plan
Flex workspace
What You’ll Be Doing
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
What We Look For
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
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.