Imaging Research Associate I

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for an Imaging Research Associate I based in the United States. As an Imaging Research Associate I, you will support the coordination and execution of clinical imaging studies from start-up through completion. You will collaborate with clinical project teams, research sites, and sponsors to ensure the accurate, timely, and compliant delivery of study data. Your work will contribute to maintaining high standards of image quality and data integrity throughout the clinical research process. You will help coordinate site onboarding, documentation, technical training, and the management of imaging data. Working in a collaborative, technology-driven environment, you will contribute to efficient study operations and reliable clinical outcomes. This role offers an opportunity to develop your expertise in clinical research while supporting the advancement of innovative medical treatments. Your attention to detail and organizational skills will help accelerate the delivery of evidence that can improve patients' lives.

Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up and the preparation of study materials. Follow up on documentation required for site qualification and coordinate logistical arrangements and technical training for site personnel. Create test-run requests for sites submitting digital data, and review, process, track, and monitor study-related data received from research sites. Identify, investigate, and help resolve data discrepancies, perform logistical edit checks, and report issues identified within study systems. Perform day-to-day image quality control (IQC) activities, including coordinating, requesting, tracking, and processing IQC data in accordance with standard operating procedures (SOPs) and study protocols. Manage communications with research sites, generate reports and queries, and verify information for accuracy before distribution. Communicate with clinical study teams and sponsors regarding study deliverables, ensuring study databases remain accurate and up to date. Prepare bone mineral density (BMD) Scan Review Forms and assist Project Managers with project administration, tracking, and reporting activities. Participate in project meetings, conference calls, and training sessions to support effective collaboration and continuous learning. Requirements: A high school diploma is required. An associate or bachelor's degree in bioscience, computer science, information technology, or a related discipline is preferred. Familiarity with PC-based computer systems and standard software applications, including Microsoft Word, Excel, email platforms, and databases. Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines is preferred. Ability to navigate computer networks, manage electronic files, and maintain accurate digital records. Strong attention to detail and organizational skills, with the ability to manage multiple tasks, adapt to changing priorities, and meet deadlines. Effective written and verbal communication skills, including the ability to interact professionally with research sites, colleagues, sponsors, and clinical study teams. Ability to work independently, take ownership of assigned responsibilities, and contribute positively to a collaborative team environment. Professional interpersonal skills, a proactive approach to problem-solving, and a commitment to accuracy, quality, and compliance. Benefits: Competitive compensation. Medical, dental, and vision insurance coverage. Remote and hybrid work options, offering flexibility in how and where work is performed. Tuition reimbursement to support continued education and professional development. Employee assistance programs and wellness resources. Life and disability insurance coverage.