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 ensure timely delivery of high-quality study data and service deliverables.

What you'll do

• 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 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.

What you'll need

• High school diploma required.
• Familiarity with PC-based computers and standard software, including Microsoft Word, Excel, email, and databases.
• 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.

Nice to have

• An Associate or Bachelor's degree in bioscience, computer science, information technology, or a related field.
• Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines.

Details

• Location: United States, remote.
• Remote and hybrid work options.