Imaging Research Associate I

🔥 8 minutes ago

🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🚫👨‍🎓 No degree required

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Clario

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1973

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 Private Equity Round on 2019-10

Healthcare Insurance • Biotechnology • Artificial Intelligence

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 from study start-up through close-out to ensure timely delivery of high-quality study outputs • Support study start-up activities, including preparation of materials and site qualification documentation follow-up • Schedule and coordinate site trainings, including logistical and technical sessions • Manage incoming study data by reviewing, processing, tracking, and monitoring submissions from clinical sites • Assist with identifying, tracking, and resolving data discrepancies in collaboration with clinical data management teams • Manage site communications, prepare reports and queries, and ensure accuracy prior to distribution • Perform daily Image Quality Control (IQC) activities, including collection, tracking, and analysis of IQC data • Coordinate baseline, interim, and end-of-study IQC processes, ensuring compliance with SOPs and protocol requirements • Support equipment-related activities such as cross-calibration, phantom data analysis, and machine equivalence documentation • Maintain study databases, including updates to site and contact information • Assist Project Managers with study planning, data tracking, and participation in project meetings and training sessions • Generate and analyze project tracking reports to identify trends, risks, and improvement opportunities • Monitor data flow, track outstanding items, and follow up with sites to ensure timelines are met • Act as a secondary point of contact for clients, sponsors, and sites, maintaining strong professional relationships • Ensure adherence to SOPs and support continuous improvement initiatives within the department

🎯 Requirements

• High School diploma required; Associate’s or Bachelor’s degree in bioscience, computer science, information technology, or related field preferred • Experience or familiarity with clinical research, drug development, or pharmaceutical environments preferred • Working knowledge of Good Clinical Practice (GCP) guidelines preferred • Proficiency with PC-based systems and standard software (e.g., Microsoft Word, Excel, databases, email platforms) • Strong attention to detail with the ability to manage and organize large volumes of data • Excellent verbal and written communication skills with strong interpersonal abilities • Ability to work independently and collaboratively in a fast-paced, deadline-driven environment • Strong problem-solving skills with the ability to identify and resolve discrepancies • Effective organizational, documentation, and prioritization skills • Self-motivated, adaptable, and able to manage changing priorities • Familiarity with file management, network navigation, and data handling best practices