This is a fully remote position, open to applicants in Hungary.

• Prepare and reproduce study materials during the start-up phase.

• Follow up on site documentation and arrange training sessions.

• Create test run requests and assess incoming study data.

• Monitor and address data discrepancies while managing site communications.

• Generate and validate reports for sites and sponsors.

• Investigate logistical edit checks and report any system issues.

• Coordinate and process IQC data, including phantom rotation and machine equivalence.

• Maintain IQC tracking databases and ensure compliance with protocols.

• Track IQC submissions and update study teams on progress.

• Maintain study databases and prepare BMD Scan Review Forms.

• Plan and coordinate activities for site start-up and training.

• Enter and track data in internal systems, participating in project meetings.

• Review project tracking, address queries, and identify site/data trends.

• Manage site communications and assist with client issue resolution.

• Respond to inquiries in a professional manner while adhering to SOP compliance.

• Participate in updates to SOPs and company-sponsored training programs.

• High school diploma is required; an Associate or Bachelor’s degree in bioscience, computer science, IT, or a related field is preferred.

• Familiarity with PC-based systems and standard software (Word, Excel, databases).

• Understanding of clinical trials and good clinical practices is preferred.

• Experience in navigating networks and managing files.

• Ability to work both independently and collaboratively; adaptable to changing priorities.

• Excellent attention to detail along with strong documentation skills.

• Effective verbal and written communication abilities.

• Professional demeanor and a positive attitude.

• Private medical coverage and MetLife protection.

• Engaging employee programs.

• Remote working options and home office allowance.

• OTP Szép Card.

Imaging Research Associate I

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