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Clairo

Clinical trial endpoint technologies and management

Imaging Research Associate 1

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeRemote in Costa RicaNo salary listedRemote

About the Job

Requirements

  • High school diploma or an Associate or Bachelor’s degree in bioscience, computer science, information technology, or a related field is preferred.
  • Familiarity with PC-based computers and standard software packages, including Word, Excel, email, and databases.
  • Knowledge of clinical trials processes and good clinical practices is preferred.
  • Ability to navigate networks and manage files effectively.
  • Ability to work independently and in a team environment with changing priorities.

Responsibilities

  • Coordinate site and operational activities throughout the study lifecycle.
  • Assist in preparing and reproducing study materials during the 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, including the study database and 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 the 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.

Desired Qualifications

  • Knowledge of clinical trials processes and good clinical practices.

About the Company

Clairo

Clinical trial endpoint technologies and management

Clario provides clinical trial endpoint technologies, including software, connected devices, and artificial intelligence to collect and analyze data across cardiac safety, eCOA, medical imaging, precision motion, and respiratory endpoints. Its platform supports site-based, hybrid, and fully decentralized trials, gathering data from devices, questionnaires, and imaging, then processing and analyzing it to produce reliable clinical evidence, with integrated training and 24/7 support. The company differentiates itself with a broad end-to-end suite plus deep regulatory expertise and a global deployment network that enables rapid localization in 100+ languages. Its goal is to simplify the clinical trial process while improving patient safety and retention, promoting patient choice and diversity, and advancing health equity by prioritizing both physical and mental well-being.

Company size
5,001-10,000
Company stage
Acquired
Total funding
$29.9M
Headquarters
London, United Kingdom
Founded
1972

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