Data Manager I

Job not on LinkedIn

🕒 July 28

🇨🇷 Costa Rica – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

📊 Data Scientist

🚫👨‍🎓 No degree required

👻 Ghost score 26%

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.

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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

• Serve as the primary internal and Sponsor contact for Data Management questions, issues, and escalations throughout the study lifecycle • Manage data collection, data cleaning, data reconciliation, database lock, and data delivery processes • Develop and maintain Data Management Plans in collaboration with Sponsors and internal stakeholders • Define study-specific data processing requirements, edit checks, and data quality standards • Collaborate with internal teams to establish study setup requirements, including visit schedules and demographic data collection • Lead development, review, approval, and maintenance of data transfer specifications and requirements • Coordinate with programming teams on data file creation, edit check development, and validation activities • Generate and review sample data files and support Sponsor approval processes for data transfers • Manage database lock activities and timelines • Serve as the primary escalation point for Data Correction Requests, queries, and Sponsor concerns • Review and approve Data Management study setup components • Maintain complete and audit-ready Data Management documentation • Conduct routine status meetings with Sponsors, CROs, and internal teams, including agenda preparation and meeting documentation • Process routine study data runs and support sample, interim, complete, and final data transfers • Identify out-of-scope requests and communicate them to Project Management for change order assessment and billing consideration • Provide study metrics and status updates for monthly reporting and project oversight

🎯 Requirements

• Bachelor’s degree in Life Sciences or a related field preferred • Minimum of 2 years of Data Management or related experience, preferably within a clinical research environment • Prior client-facing experience preferred • Strong understanding of clinical trial processes and data management principles • Proficiency with Microsoft Office applications • Strong organizational, interpersonal, time-management, and problem-solving skills • Ability to manage multiple priorities and meet deadlines in a dynamic environment • High attention to detail and commitment to data quality and accuracy • Exposure to SAS and/or SQL preferred • Knowledge of CDISC SDTM standards preferred • Excellent written and verbal communication skills in English • Ability to collaborate effectively with Sponsors, programmers, project teams, and other cross-functional stakeholders

🏖️ Benefits

• Competitive compensation • Comprehensive health, dental, and vision coverage • Retirement savings plan with company contribution • Paid time off and company holidays