Clinical Data Associate II

Role: Support Clinical Data Management activities for assigned studies, ensuring data quality, compliance, and documentation according to industry standards. Responsibilities: review CRFs, support data system testing and maintenance (EDC, IRT, ePRO), perform data checks, queries, and reconciliation, prepare data listings and metrics, and escalate issues as needed. Collaborate cross-functionally and adhere to GxP, ICH, CDISC, and 21 CFR Part 11 standards. Requirements: minimum 1 year (preferably 2+) in Clinical Data Management, Bachelor's in a scientific or medical field, strong communication, and proficiency in MS Office. Preferred: experience with data system design, data review plans, and data entry systems. High-Value: focus on clinical data management within biopharma, supporting phases of clinical trials, with emphasis on data quality and regulatory compliance. WorkSetup: not specified; salary range $75,000–$90,000.