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High due to Tier-1 brand, metro location, and open associate-level data role attracting many applicants.
Clinical data management requires GCP and regulatory expertise, limiting cross-industry transferability.
Mandatory ICH/GCP and electronic documentation system experience but no strict years requirement.
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Engage in clinical data monitoring and management activities including data review, query management, and investigation of logic check flags.
Ensure quality and integrity of clinical trial databases via documentation, testing, validation, and implementation of data collection tools.
Serve as first point of contact for Clinical Trial Management System (CTMS) queries and collaborate with study teams to resolve data and documentation discrepancies.
Bachelor's degree (BA/BS) with any years of experience.
Demonstrated experience with ICH/GCP documentation requirements.
Hands-on experience with electronic documentation management systems or web-based data management systems.
Strong oral and written English communication skills; proficiency in Microsoft Office Suite.
Familiarity with clinical trial management systems (CTMS) and clinical development processes.
Experience with data validation, quality control, and regulatory data standards.
Ability to leverage AI tools (e.g., ChatGPT, Microsoft Copilot) for problem solving and productivity enhancement, with understanding of responsible AI use.