Clinical Data Associate II

🔥 2 hours ago

🇦🇷 Argentina – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

✨ Associate

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Perform data cleaning activities, including query review and closure, to support data quality and study timelines • Review database pages and identify data issues to ensure accurate and complete clinical trial records • Prepare and distribute study-specific data management metrics to internal and external stakeholders • Conduct User Acceptance Testing (UAT) of EDC databases • Review third-party vendor data reconciliations and help resolve discrepancies • Perform Database Quality Assessment (DQA) reviews • Review SAS listings and data checks, taking appropriate action on queries and findings • Prepare end-of-study media and documentation for trial archival activities • Submit final study documents to the Trial Master File

🎯 Requirements

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, a related discipline, or equivalent relevant experience • Minimum of 1 year of relevant industry experience in clinical research, data management, or a related field • Proficiency in English • Experience with clinical data cleaning, query review and closure • Experience reviewing database pages and identifying data issues • Experience preparing study-specific data management metrics • Experience conducting User Acceptance Testing (UAT) of EDC databases • Experience with third-party vendor data reconciliations • Experience performing Database Quality Assessment (DQA) reviews • Experience reviewing SAS listings and data checks • Experience preparing end-of-study media and documentation • Experience submitting final study documents to the Trial Master File

🏖️ Benefits

• Equal employment opportunities • Diverse and inclusive work environment • Collaboration and creativity-focused workplace • Supportive and cohesive teams • Accessible leadership • Opportunity to work with global teams across multiple time zones