Over Senior Analyst, bringing a strong foundation in data integrity, time management, and regulatory compliance. Skilled in monitoring updates to pharmacopoeias and standard operating procedures to ensure continued adherence to industry standards. Possess approximately one year of hands-on experience in Computer System Validation (CSV), with a solid understanding of GxP and data lifecycle requirements.
Currently serving as an In-Process Control Supervisor in the CRO (Clinical Research Organization) field, with proven success in supervisory responsibilities, regulatory compliance, and workflow oversight. Adept at leading teams, ensuring operational efficiency, and maintaining high quality standards in a regulated environment.