Imaging Research Associate I

Clario

28d•Hybrid

About The Position

Clario, a part of Thermo Fisher Scientific, is seeking an Imaging Research Associate I to support the coordination of site and operational activities across the full lifecycle of clinical imaging studies. In this role, you will work closely with project teams, sites, and sponsors to ensure the timely delivery of high-quality study data and service deliverables. This position plays an important role in supporting compliant, efficient clinical research operations that help bring life-changing therapies to patients faster.

Requirements

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 Haves

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

Responsibilities

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.