Imaging Research Associate I

Overview

Coordinate site and operational activities across the full lifecycle of clinical imaging studies, working with project teams, sites and sponsors to deliver high-quality study data and service deliverables.

What you'll do

• 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 you'll need

• Familiarity with PC-based computers and standard software packages (Word, Excel, email, databases)
• 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

Nice to have

• High school diploma or Associate/Bachelor's degree in bioscience, computer science, information technology, or related field
• Knowledge of clinical trials process and good clinical practices

Details

• Location: Costa Rica, remote