Clario’s medical imaging expertise is unparalleled to any other medical imaging core lab in the industry, and we're looking to hire Imaging Research Associates for our growing imaging operations team in Budapest.

What We Offer

Competitive compensation
Attractive benefits (security, flexibility, support and well-being)
Engaging employee programs
Flexible hybrid working model
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What You'll Be Doing

The Imaging Research Associate I, coordinates all site and operational activities, from study start to study close, to ensure the timely delivery of high quality service deliverables for assigned studies.

Assist in preparation and reproduction of study materials during study start-up phase of clinical trials
Follow up with outstanding documentations from clinical sites 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 the monitoring and resolution of data discrepancies resulting from discrepancy listings generated from clinical data management
Manage site communications, generate site and patient reports and queries, and verify reports prior to distribution to clinical sites and sponsors
Investigate and complete logistical edit checks
Report issues found with study systems (i.e. study database, reading analysis system)
Perform day to day IQC activities including coordinating, requesting, tracking and processing of IQC data including:
Baseline, on-going, and end/interim analysis IQC Data Review
Coordination of cross calibration phantom rotation
Phantom data analysis and data entry
Ensuring accuracy of tracking information in IQC Tracking and study tracking databases as pertaining to IQC and/or DXA scanner information
Coordinating machine change instances for appropriate documentation and equivalence data collection
Machine Equivalence analysis and processing
Ensure IQC data is collected and maintained according to applicable SOPs and/or study protocol requirements
Manage Baseline, Interim and End of Study IQC data submissions, track and report progress to study teams and ensure timelines are met
Communicate with Clario clinical study team and/or sponsor regarding deliverables
Understand functions of software used to produce and collect IQC data
BMD Scan Review Form preparation
Study database maintenance (e.g., change of contact information)

Assists Project Managers with project administration by

Planning and coordinating the site start-up activities
Reading and understanding project protocol documents
Entering, maintaining, and tracking of data in internal software
Participating in project meetings, conference calls, and training calls

Assists Project Managers in maintaining, reviewing and communicating project progress by

Reviewing and analysing project tracking weekly
Generates, tracks and resolves data queries
Identifying site and data trends, and recommending actions to Project Manager
Communicating and following up on project tracking discrepancies
Assisting in monitoring data flow
Generating, reviewing and distributing weekly/monthly project tracking reports
Ensures the development and adherence to project timelines as they relate to therapeutic processes by
Following up on outstanding items including missing data, incomplete paperwork, etc.
Managing site communication, including distribution of subject data reports
Assisting in tracking and resolving of client issues
Scheduling and tracking completion of site training
Serving as additional point of contact to client, sites, sponsors, etc.
Keeping supervisor advised of current issues

Maintains client (internal and external) satisfaction by

Responding to inquiries in a professional, courteous and timely manner

Maintains Quality Service and Departmental Standards by

Reading, understanding and adhering to organizational Standard Operating Procedures (SOPs)
Assisting in establishing and enforcing departmental standards
Participating in the modification of company SOPs related to the therapeutic team

Maintains Technical and Industry Knowledge by

Attending and participating in applicable company-sponsored training

What We Look For

Bachelors Degree in Life Sciences or similar
Familiarity with PC-based computers and standard software packages including e-mail, word processors, Excel spreadsheets and databases.
Knowledge of the drug development/clinical trials process/basic clinical research and/or experience working in a pharmaceutical environment preferred
Knowledge of “good clinical practices” preferred

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Clario jobs

Imaging Research Associate