Imaging Research Associate I

Clario

Imaging Research Associate I at Clario coordinating study activities and ensuring data integrity. Supporting clinical trials with high-quality imaging expertise within a global team environment.

Posted 6/29/2026full-timeRemote • 🇭🇺 HungaryJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing clinical trial documentation, ensuring protocol compliance, and maintaining study databases. Proficient in data tracking, report generation, and effective communication with study teams and clients.

Highest-signal resume keywords

Clinical Trials KnowledgeData ManagementDocumentation SkillsCommunication SkillsSOP Compliance

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data TrackingReport GenerationDatabase ManagementLogistical Edit ChecksStudy Material PreparationTest Run RequestsIQC Data CoordinationProtocol ComplianceSite Start-Up ActivitiesBMD Scan Review Forms

Soft Skills

Attention to DetailAdaptabilityTeam CollaborationProfessional AttitudeEffective Communication

Tools & Technologies

PC-Based SystemsMicrosoft WordMicrosoft ExcelDatabases

Industry Keywords

Good Clinical PracticesClinical TrialsSOP UpdatesSite CommunicationsClient Issue Resolution

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

Private medical coverage and MetLife protection
Engaging employee programs
Remote working & home office allowance
OTP Szép Card