Imaging Study Coordinator | Remote Options & Tuition Support

eResearch Technology Inc; United States; Hybrid; USD 50,000 - 70,000; Full time

Benefits offered by this job

Competitive pay

Health insurance

Remote & Hybrid

Tuition reimbursement

Wellness programs

Life and disability insurance

Job summary

Clario is seeking an Imaging Research Associate I to coordinate site and operational activities across the full lifecycle of clinical imaging studies. You will work with project teams, sites, and sponsors to ensure timely delivery of high-quality study data and services.

In this role, you will support compliant, efficient clinical research operations and maintain accurate information within study databases. Strong attention to detail and collaboration skills are essential.

Qualifications

• High school diploma required.
• Associate or Bachelor’s degree preferred (bioscience, IT, or related).
• Familiarity with PC-based computers and Microsoft Office (Word/Excel).
• Knowledge of clinical trial processes and GCP guidelines preferred.
• Ability to navigate computer networks and manage electronic files.

Responsibilities

• Coordinate site and operational activities across the clinical imaging study lifecycle.
• Follow up on required documentation to support site qualification and schedule training.
• Create test-run requests and review data from sites.
• Monitor and resolve data discrepancies and perform IQC data processing.
• Manage site communications, generate reports, and verify accuracy before distribution.
• Communicate with clinical study teams and sponsors regarding deliverables.
• Prepare BMD Scan Review Forms and support project administration, tracking, and reporting.
• Participate in project meetings, calls, and training sessions.

Skills

Attention to detail

Communication skills

Team collaboration

Independent work

Education

High school diploma

Associate degree

Bachelor’s degree

Tools

MS Word

MS Excel

Email

Databases

Job description

Clario is seeking an Imaging Research Associate I to coordinate site and operational activities across the full lifecycle of clinical imaging studies. You will work with project teams, sites, and sponsors to ensure timely delivery of high-quality study data and services.

In this role, you will support compliant, efficient clinical research operations and maintain accurate information within study databases. Strong attention to detail and collaboration skills are essential.