Imaging Research Associate I

Clario

. Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up activities and preparation of study materials .

Posted 10/12/2026full-timeRemote • United StatesJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating clinical imaging study activities, ensuring compliance with Good Clinical Practice (GCP) guidelines, and managing data quality control processes. Proficient in effective communication and collaboration with clinical study teams and site personnel.

Highest-signal resume keywords

Clinical Trial ProcessesGood Clinical Practice (GCP)Data Quality ControlMicrosoft WordMicrosoft Excel

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ManagementImage Quality Control (IQC)Study Protocol ComplianceDocumentation ManagementLogistical Training Coordination

Soft Skills

Attention to DetailOrganizational SkillsVerbal CommunicationWritten CommunicationInterpersonal Skills

Tools & Technologies

PC-Based ComputersDatabasesEmail

Industry Keywords

Clinical Imaging StudyStudy LifecycleSite QualificationBone Mineral Density (BMD)Standard Operating Procedures (SOPs)

About the role

Key responsibilities & impact

Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up activities and preparation of study materials
Follow up on required documentation to support site qualification and schedule logistical and technical training with site personnel
Create test-run requests for sites submitting digital data and review, process, track, and monitor study-related data received from sites
Monitor and resolve data discrepancies, conduct logistical edit checks, and report issues identified within study systems
Perform day-to-day image quality control (IQC) activities, including coordinating, requesting, tracking, and processing IQC data in accordance with standard operating procedures (SOPs) and study protocol requirements
Manage site communications, generate reports and queries, and verify information for accuracy before distribution
Communicate with clinical study teams and sponsors regarding study deliverables and maintain accurate information within the study database
Prepare bone mineral density (BMD) Scan Review Forms and support Project Managers with project administration, tracking, and reporting
Participate in project meetings, conference calls, and training sessions

Requirements

What you’ll need

High school diploma required
Associate or Bachelor’s degree in bioscience, computer science, information technology, or a related field is preferred
Familiarity with PC-based computers and standard software, including Microsoft Word, Excel, email, and databases
Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines is preferred
Ability to navigate computer networks and manage electronic files effectively
Strong attention to detail, organization, and ability to manage changing priorities and deadlines
Clear verbal and written communication skills and the ability to collaborate effectively with colleagues, sites, and study teams
Ability to work independently while contributing effectively in a team environment
Professional interpersonal skills and the ability to take ownership of assigned responsibilities

Benefits

Comp & perks

Competitive compensation
Medical, dental, and vision coverage
Remote and hybrid work options
Tuition reimbursement
Employee assistance and wellness programs
Life and disability insurance