Imaging Research Associate I

<h3>Accountabilities:</h3><li>Coordinate site and operational activities throughout the clinical imaging study lifecycle, including study start-up and the preparation of study materials.</li><li>Follow up on documentation required for site qualification and coordinate logistical arrangements and technical training for site personnel.</li><li>Create test-run requests for sites submitting digital data, and review, process, track, and monitor study-related data received from research sites.</li><li>Identify, investigate, and help resolve data discrepancies, perform logistical edit checks, and report issues identified within study systems.</li><li>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.</li><li>Manage communications with research sites, generate reports and queries, and verify information for accuracy before distribution.</li><li>Communicate with clinical study teams and sponsors regarding study deliverables, ensuring study databases remain accurate and up to date.</li><li>Prepare bone mineral density (BMD) Scan Review Forms and assist Project Managers with project administration, tracking, and reporting activities.</li><li>Participate in project meetings, conference calls, and training sessions to support effective collaboration and continuous learning.</li><h2>Requirements:</h2><li>A high school diploma is required. An associate or bachelor's degree in bioscience, computer science, information technology, or a related discipline is preferred.</li><li>Familiarity with PC-based computer systems and standard software applications, including Microsoft Word, Excel, email platforms, and databases.</li><li>Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines is preferred.</li><li>Ability to navigate computer networks, manage electronic files, and maintain accurate digital records.</li><li>Strong attention to detail and organizational skills, with the ability to manage multiple tasks, adapt to changing priorities, and meet deadlines.</li><li>Effective written and verbal communication skills, including the ability to interact professionally with research sites, colleagues, sponsors, and clinical study teams.</li><li>Ability to work independently, take ownership of assigned responsibilities, and contribute positively to a collaborative team environment.</li><li>Professional interpersonal skills, a proactive approach to problem-solving, and a commitment to accuracy, quality, and compliance.</li><h2>Benefits:</h2><li>Competitive compensation.</li><li>Medical, dental, and vision insurance coverage.</li><li>Remote and hybrid work options, offering flexibility in how and where work is performed.</li><li>Tuition reimbursement to support continued education and professional development.</li><li>Employee assistance programs and wellness resources.</li><li>Life and disability insurance coverage.</li>