Imaging Research Associate I

🔥 3 minutes ago

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of Clario

Clario

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

• Prepare and reproduce study materials during start-up • Follow up on site documentation and schedule training sessions • Create test run requests and review incoming study data • Monitor and resolve data discrepancies and manage site communications • Generate and verify reports for sites and sponsors • Investigate logistical edit checks and report system issues • Coordinate and process IQC data including phantom rotation and machine equivalence • Maintain IQC tracking databases and ensure protocol compliance • Track IQC submissions and communicate progress to study teams • Maintain study databases and prepare BMD Scan Review Forms • Plan and coordinate site start-up activities and training • Enter and track data in internal systems and participate in project meetings • Review project tracking, resolve queries, and identify site/data trends • Manage site communications and assist with client issue resolution • Respond to inquiries professionally and maintain SOP compliance • Participate in SOP updates and company-sponsored training

🎯 Requirements

• High school diploma required; Associate/Bachelor’s degree in bioscience, computer science, IT or related field preferred • Familiarity with PC-based systems and standard software (Word, Excel , databases) • Understanding of clinical trials and good clinical practices preferred • Experience navigating networks and managing files • Ability to work independently and in teams; adaptable to changing priorities • Excellent attention to detail and strong documentation skills • Effective verbal and written communication skills • Professional and positive attitude

🏖️ Benefits

• Private medical coverage and MetLife protection • Engaging employee programs • Remote working & home office allowance • OTP Szép Card

Apply Now