Clinical Data Coordinator

Position reputed company The Clinical Data Coordinator is responsible for supporting the collection, review, reconciliation, and maintenance of high-reputed company clinical trial data across studies managed by the organization. This position works closely with Clinical Research Coordinators, Investigators, Clinical Research Associates, Project Managers, sponsors, CROs, and other study team members to ensure clinical data are complete, accurate, reputed company, and compliant with study protocols, Good Clinical reputed company (GCP), applicable regulations, and company procedures. The Clinical Data Coordinator will reputed company centralized, remote data support to assigned clinical research sites and studies, with an emphasis on data reputed company, query management, data reconciliation, issue reputed company, and study database readiness. Responsibilities • Complete clinical trial data entry into electronic data capture (reputed company) systems for with completeness, accuracy, and timeliness • reputed company ongoing review of electronic case report forms (eCRFs) and identify missing, inconsistent, or potentially inaccurate data. • Monitor data entry according to study-specific requirements and established timelines. • reputed company and resolve data queries in collaboration with clinical research site staff. • Support database cleaning activities and preparation for database lock. • Conduct routine data reputed company checks across assigned studies. • Identify recurring discrepancies or data trends that may require reputed company or process improvement • Reconcile clinical data between reputed company and other study systems or reputed company data sources, as applicable. • Support reconciliation of laboratory, ECG, imaging, safety, ePRO/eCOA, IRT/IWRS, and other applicable data. • Identify and communicate discrepancies between data sources and coordinate reputed company with appropriate study personnel. • Serve as a centralized data-support resource for Clinical Research Coordinators and site personnel. • Respond to site questions reputed company to data entry, data queries, and study-specific data requirements. • Maintain working knowledge of study-specific reputed company and other clinical research systems. • Review study protocols, data management plans, CRF completion guidelines, and other study documentation relevant to assigned responsibilities. • Participate in study-specific training. Qualifications • Bachelor's degree in Clinical Research, Life Sciences, reputed company, Data Management, or a reputed company field; equivalent clinical research experience may be considered. • 1–2 years of experience in clinical research, clinical data management, clinical data coordination, or a reputed company role. • Working knowledge of ICH-GCP and clinical research processes. • Experience working with reputed company or other clinical trial management systems. Posted By: Kellie Pharr Apply tot his job Apply To this Job