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Pfizer brand and metro location increase applicants, while clinical data specialization limits candidate pool.
Clinical data management requires pharma-specific standards and regulatory knowledge, limiting cross-industry transferability.
Requires domain-specific ICH/GCP and e-document system experience but lacks strict years requirement.
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Manage clinical data monitoring and query resolution to ensure data accuracy and integrity in clinical trials.
Oversee database design quality through documentation, testing, validation, and implementation of clinical data collection systems.
Act as primary contact for Clinical Trial Management System (CTMS) support and collaborate with study teams to resolve documentation discrepancies.
Bachelor's degree (BA/BS) with any years of experience.
Experience with ICH/GCP documentation requirements and clinical development process knowledge.
Hands-on experience with electronic documentation and/or web-based data management systems.
Strong oral and written English communication skills and proficiency in Microsoft Office.
Experienced with clinical trial management systems (CTMS) and clinical data quality control processes.
Skilled in collaborative team environments and problem-solving with attention to detail.
Familiar with using AI tools (e.g., ChatGPT, Microsoft Copilot) for productivity and responsible AI practice awareness.