Clario

Imaging Research Associate I

Costa Rica · Work style not stated · Full time

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About the role

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EmployerClario
LocationCosta Rica
Work styleWork style not stated
Employment typeFull time
Employer posted5 Oct 2026

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

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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.

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