At Clario, part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision‑making in highly controlled regulatory environments.
As Imaging Research Associate I, you will join Clario’s Medical Imaging team in Hungary and help advance clinical trials through high-quality imaging data. In this role, you’ll coordinate site and operational activities from study start to close, ensuring timely delivery of service deliverables and supporting data integrity across global studies.
What We Offer
Competitive compensation and incentives
Private medical coverage and MetLife protection
Engaging employee programs
Remote working & home office allowance
OTP Szép Card
What You’ll Be Doing
Prepare and reproduce study materials during start-up
Follow up on site documentation and schedule training sessions
Create test run requests and review incoming study data
Monitor and resolve data discrepancies and manage site communications
Generate and verify reports for sites and sponsors
Investigate logistical edit checks and report system issues
Coordinate and process IQC data including phantom rotation and machine equivalence
Maintain IQC tracking databases and ensure protocol compliance
Track IQC submissions and communicate progress to study teams
Maintain study databases and prepare BMD Scan Review Forms
Plan and coordinate site start-up activities and training
Enter and track data in internal systems and participate in project meetings
Review project tracking, resolve queries, and identify site/data trends
Manage site communications and assist with client issue resolution
Respond to inquiries professionally and maintain SOP compliance
Participate in SOP updates and company-sponsored training
What We Look For
High school diploma required; Associate/Bachelor’s degree in bioscience, computer science, IT or related field preferred
Familiarity with PC-based systems and standard software (Word, Excel, databases)
Understanding of clinical trials and good clinical practices preferred
Experience navigating networks and managing files
Ability to work independently and in teams; adaptable to changing priorities
Excellent attention to detail and strong documentation skills
Effective verbal and written communication skills
Professional and positive attitude
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.