Imaging Research Associate I

🔥 0 minutes ago

🇭🇺 Hungary – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🚫👨‍🎓 No degree required

👻 Ghost score 10%

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Clario

WebsiteLinkedInAll Job Openings

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 imaging site and operational activities throughout the study lifecycle, from startup through closeout. • Support site qualification activities by collecting, reviewing, and tracking required study documentation. • Schedule and coordinate site training, technical training, and onboarding activities. • Assist with the preparation, distribution, and maintenance of study materials and site communications. • Review, process, track, and monitor imaging and study-related data received from clinical sites. • Generate and manage site reports, patient reports, queries, and communications for sponsors and study teams. • Investigate, track, and support resolution of data discrepancies and logistical edit checks. • Monitor study systems and escalate issues related to databases, imaging platforms, and analysis systems. • Perform imaging quality control activities, including collection, review, tracking, and processing of imaging quality control data. • Coordinate cross-calibration phantom activities, scanner qualification processes, machine changes, and equivalency assessments. • Support image quality monitoring through data analysis, data entry, and documentation review. • Maintain imaging quality control tracking systems and study databases to ensure accurate and complete records. • Assist Project Managers with study startup planning, project administration, project tracking, and operational coordination. • Participate in project meetings, sponsor calls, training sessions, and internal study discussions. • Generate and distribute project tracking reports while monitoring study progress, timelines, and deliverables. • Identify trends, risks, and issues related to site performance and data quality and communicate recommendations to project leadership. • Support resolution of client and site issues while maintaining a high level of customer service and responsiveness. • Contribute to continuous improvement initiatives, departmental standards, and process enhancements.

🎯 Requirements

• High school diploma required. • Associate's degree or Bachelor's degree in Bioscience, Computer Science, Information Technology, Healthcare, Life Sciences, or a related field preferred. • Experience within clinical research, healthcare, imaging operations, pharmaceutical services, or a related industry preferred. • Understanding of clinical trial processes, drug development, Good Clinical Practice (GCP), or regulated environments is advantageous. • Familiarity with Microsoft Office applications, including Word, Excel, Outlook, and database systems. • Ability to navigate file systems, maintain accurate documentation, and manage electronic records. • Strong organizational and time-management skills with the ability to manage multiple priorities and deadlines. • Excellent attention to detail and commitment to delivering high-quality work. • Strong verbal and written communication skills with the ability to communicate effectively in English. • Demonstrated ability to work both independently and collaboratively within cross-functional teams. • Customer-focused mindset with the ability to build productive relationships with sites, sponsors, and internal stakeholders. • Strong analytical, problem-solving, and documentation skills. • Self-motivated, goal-oriented, and adaptable in a fast-paced environment.

🏖️ Benefits

• Competitive compensation and incentives. • Private medical coverage and MetLife protection. • SZÉP Card and telework reimbursement. • Engaging employee events and hybrid technology support.