Imaging Research Associate I

Clario; United States; Remote; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive compensation

Private health insurance

Engaging employee programs

Flexible work schedules

Attractive PTO plan

Flex workspace

Job summary

Clario is seeking an Imaging Research Associate I to support coordination of 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 study data and services, helping drive compliant and efficient clinical research operations that bring therapies to patients faster.

Qualifications

• High school diploma or equivalent required or preferred
• Familiarity with PC-based computers and standard software packages (Word, Excel, email, databases)
• Knowledge of clinical trials process and good clinical practices preferred
• 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 with changing priorities
• Professional, positive attitude and strong interpersonal skills
• Leadership qualities and ability to meet aggressive deadlines

Responsibilities

• 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

Skills

Attention to detail

Communication skills

Independent work

Teamwork

Leadership

Clinical trials knowledge

IT literacy

Education

High school diploma or equivalent

Associate/Bachelor’s degree in bioscience/IT

Tools

MS Word

Excel

Email

Databases

Job description

Clario, 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.

What We Offer

• Competitive compensation

• Private health insurance

• Engaging employee programs

• Flexible work schedules

• Attractive PTO plan

• Flex workspace

What You’ll Be Doing

• 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 We Look For

• High school diploma or Associate/Bachelor’s degree in bioscience, computer science, information technology, or related field preferred

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

• Knowledge of clinical trials process and good clinical practices preferred

• 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

At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you’re advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life‑changing therapies to patients faster.