Highly analytical Clinical Data Management professional transitioning from Histotechnology, with 5+ years of laboratory experience in specimen processing, quality assurance, and laboratory information systems. Recently achieved Clinical Data Management Certification from the Society of Clinical Data Management (SCDM), gaining expertise in clinical trial data collection, database management, regulatory compliance (GCP, FDA, ICH), and data integrity. Proficient in LIS, Soft Path, EPIC, and electronic data capture (EDC) systems, ensuring accurate and efficient data handling for clinical trials. Adept at working cross-functionally with clinical teams, data analysts, and regulatory bodies to maintain high-quality, compliant clinical trial data. Committed to leveraging laboratory expertise and data management skills to enhance clinical research outcomes and improve patient care.
Key Responsibilities:
Specimen Preparation & Processing:
Staining & Slide Preparation:
Laboratory Equipment & Maintenance:
Quality Control & Compliance:
Data Management & Reporting:
Key responsibilities :