Imaging Research Associate I

🕒 May 5

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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 study close to support high‑quality study delivery • Assist with preparation and distribution of study materials and follow up on outstanding site documentation • Schedule and coordinate logistical and technical trainings for clinical site personnel • Review, process, track, and monitor imaging and study‑related data received from sites • Support identification, tracking, and resolution of data discrepancies and logistical edit checks • Perform day‑to‑day Imaging Quality Control (IQC) activities, including baseline, interim, and end‑of‑study IQC data review • Coordinate phantom rotations, analyze phantom data, and ensure accurate data entry and tracking • Support machine change documentation, equivalence data collection, and machine equivalence analysis • Maintain study databases and tracking systems, ensuring data accuracy and compliance with SOPs and protocols • Generate, review, and distribute site, patient, and project tracking reports • Communicate with internal study teams, sites, and sponsors regarding deliverables and timelines • Assist Project Managers with site start‑up activities, project tracking, data flow monitoring, and issue resolution • Participate in project meetings, training calls, and cross‑functional discussions.

🎯 Requirements

• High School Diploma required; Associate’s or Bachelor’s degree in bioscience, computer science, information technology, or a related field preferred • Familiarity with PC‑based systems and standard software tools (email, word processing, Excel, databases) • Basic understanding of clinical trials, drug development, or pharmaceutical research preferred • Knowledge of Good Clinical Practices (GCP) preferred • Strong attention to detail, organizational skills, and documentation practices • Ability to work independently and collaboratively in a fast‑paced, deadline‑driven environment • Clear verbal and written communication skills and a professional, service‑oriented mindset.

🏖️ Benefits

• Competitive compensation aligned to the local market • Comprehensive benefits package in accordance with Costa Rica employment standards • Exposure to global clinical trials and cross‑functional collaboration • Structured onboarding, training, and professional development opportunities • A collaborative, quality‑driven, and inclusive work environment.