Imaging Research Associate I

🔥 12 hours ago

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🚫👨‍🎓 No degree required

🦅 H1B Visa Sponsor

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Logo of Clario

Clario

5001 - 10000 employees

Founded 1973

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 Private Equity Round on 2019-10

Healthcare • Consulting • Logistics

Clario is a company specializing in accelerating clinical trials from initiation to implementation through advanced technologies and services. Since 2018, Clario has revolutionized endpoint analyses in clinical trials by integrating over 30 artificial intelligence-enabled solutions across more than 600 active trials, enhancing data quality and patient privacy while expediting data collection processes. Clario provides a comprehensive clinical trial management platform, offering solutions such as eCOA, cardiac safety, medical imaging, precision motion, and respiratory services in various therapeutic areas including oncology, cardiology, and neurology. Known for its global reach, Clario supports clinical trials in over 100 countries with a strong focus on decentralized and hybrid trial models. The company's commitment to patient safety and innovation is reflected in their over 26,000 trials and involvement in numerous new drug approvals.

📋 Description

• 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 (IQC) activities, including coordinating, requesting, tracking, and processing IQC data in accordance with standard operating procedures (SOPs) 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 (BMD) Scan Review Forms and support Project Managers with project administration, tracking, and reporting • Participate in project meetings, conference calls, and training sessions

🎯 Requirements

• High school diploma required • Associate or Bachelor’s degree in bioscience, computer science, information technology, or a related field is preferred • Familiarity with PC-based computers and standard software, including Microsoft Word, Excel, email, and databases • Knowledge of clinical trial processes and Good Clinical Practice (GCP) guidelines is preferred • Ability to navigate computer networks and manage electronic files effectively • Strong attention to detail, organization, and 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

🏖️ Benefits

• Competitive compensation • Medical, dental, and vision coverage • Remote and hybrid work options • Tuition reimbursement • Employee assistance and wellness programs • Life and disability insurance

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