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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 USANo salary listedRemote

About the Job

Requirements

  • A high school diploma is 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 and organization, with the 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.

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 activities, including coordinating, requesting, tracking, and processing IQC data in accordance with standard operating procedures 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 scan review forms and support project managers with project administration, tracking, and reporting.
  • Participate in project meetings, conference calls, and training sessions.

Desired Qualifications

  • 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 guidelines is preferred.

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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