Imaging Research Associate I

🕒 July 1

🇨🇷 Costa Rica – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🔬 Research Analyst

🚫👨‍🎓 No degree required

👻 Ghost score 37%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

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

Upload Resume

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 site and operational activities throughout the study lifecycle • Assist in preparation and reproduction of study materials during start-up phase • Follow up on outstanding documentation to complete site qualification • Schedule logistical and technical trainings with site personnel • Create test run requests for sites submitting digital data • Review, process, track, and monitor all study-related data received from sites • Assist in monitoring and resolving data discrepancies from clinical data management • Manage site communications, generate reports and queries, and verify accuracy before distribution • Investigate and complete logistical edit checks • Report issues found with study systems, including study database and reading analysis system • Perform day-to-day IQC activities, including coordinating, requesting, tracking, and processing IQC data • Ensure IQC data is collected and maintained according to SOPs and study protocol requirements • Communicate with clinical study teams and sponsors regarding deliverables • Maintain study database and prepare BMD Scan Review Forms • Support Project Managers with project administration, tracking, and reporting • Participate in project meetings, conference calls, and training sessions

🎯 Requirements

• High school diploma or Associate/Bachelor’s degree in bioscience, computer science, information technology, or related field preferred • Familiarity with PC-based computers and standard software packages (Word, Excel, email, databases) • Knowledge of clinical trials process and good clinical practices preferred • Ability to navigate networks and manage files effectively • Strong attention to detail and organizational skills • Excellent verbal and written communication skills • Ability to work independently and in a team environment with changing priorities • Professional, positive attitude and strong interpersonal skills • Leadership qualities and ability to meet aggressive deadlines

🏖️ Benefits

• Competitive compensation • Private health insurance • Engaging employee programs • Flexible work schedules • Attractive PTO plan • Flex workspace