Clario
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.
Associate Data Manager
🔥 0 minutes ago
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Clario
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
• Perform quality control and consistency checks on study data outputs, ensuring accuracy between source data, edit check outputs, and final deliverables. • Investigate data discrepancies and collaborate with Data Managers, scientific teams, and medical staff to facilitate issue resolution and documentation. • Support the creation, maintenance, and review of study documentation, including Data Management Plans, Data Transfer Specifications, and related deliverables. • Coordinate updates to Clinical Data Management task schedules, including edit checks, transfer schedules, reconciliation activities, and final data transfer requirements. • Assist with data management metrics, study tracking activities, and maintenance of accurate study assignment information within applicable systems. • Support the preparation, formatting, and maintenance of data management documents, templates, reports, and presentations. • Serve as a primary point of contact for client reconciliation feedback, ensuring timely investigation, follow-up, and resolution of data-related requests. • Maintain high-quality documentation and audit-ready records relating to reconciliation activities and study data management processes. • Communicate project status updates effectively to internal teams, project leadership, and clients. • Assist in the maintenance, storage, and organization of study documentation throughout the project lifecycle. • Contribute to continuous improvement initiatives focused on workflow optimization, quality enhancement, and process efficiency. • Support Corrective and Preventive Action activities related to study-specific data management processes.
🎯 Requirements
• Bachelor’s, Master’s, or PhD degree in Life Sciences, Healthcare, Pharmaceutical Sciences, Clinical Research, Data Science, or a related field, or equivalent practical experience. • Experience within the pharmaceutical, biotechnology, healthcare, life sciences, or clinical research industry preferred. • Foundational understanding of Clinical Data Management principles and the role of data management within clinical trials. • Ability to review, interpret, and understand clinical trial protocols, study documentation, and sponsor requirements. • Knowledge of Good Clinical Practice, FDA, EMA, and other applicable regulatory requirements preferred. • Exposure to eClinical technologies such as eCOA, ePRO, eConsent, RTSM/IRT, or related clinical systems highly desirable. • Previous experience in clinical research roles such as Clinical Research Associate, Study Coordinator, Project Assistant, Project Coordinator, Clinical Trial Assistant, or similar positions preferred. • Familiarity with SAS, SQL, or other data analysis and reporting tools highly desirable. • Knowledge of CDISC standards, including SDTM, considered an advantage. • Strong analytical, organizational, and problem-solving skills with exceptional attention to detail. • Excellent written and verbal communication skills and the ability to work effectively within cross-functional global teams. • Ability to manage multiple priorities and deliver high-quality work in a deadline-driven environment.
🏖️ Benefits
• Competitive compensation and incentives • Private medical coverage and MetLife protection • SZÉP Card and telework reimbursement • Flexible time off • Engaging employee events • Hybrid technology support
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