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PharPoint Research, Inc. logo
September 16, 2026
Full-time
Remote friendly (Durham, NC)
Worldwide
Clinical Research and Development
Role: Clinical Data Management Specialist responsible for executing data management functions in clinical trials. Objectives include ensuring data accuracy, quality, and compliance across multiple protocols. Responsibilities encompass data entry, reconciliation, quality control, query management, database coding, and protocol-specific documentation such as case report forms and Data Management Plans. The role provides functional oversight and mentorship to interns and staff, with involvement in staffing, training, and performance evaluation. Qualifications: Associate’s degree or higher in a scientific or related field, with at least 1 year of clinical data management experience; familiarity with relational databases and data management systems; knowledge of clinical trial data processes. Preferred: Bachelor’s degree; experience with GxP environments. High-value specifics: Hands-on data management in clinical trial settings, with emphasis on data quality and integrity; no specific therapeutic areas or modalities specified; general office environment; no travel requirements noted.