Dedicated and detail-oriented clinical research professional with over three years of industry expertise, specializing in data collection, management, and regulatory compliance. Proficient in utilizing various eCRF platforms, including MEDIDATA RAVE, ORACLE INFORM, and more. Experienced in dossier preparation, informed consent, case report form, and advanced software tools like IBM SPSS and PHILIPS DICOM VIEWER. Demonstrated ability to manage queries, assess risks, and report serious adverse events with successful resolution. Adept in Good Documentation Practice (GDP), ICH, FDA, and Division 5 compliance. Proven track record in supporting multicentric and global studies, ensuring data integrity, and maintaining high participant safety and welfare standards. Recognized for excellent communication, data entry, and team collaboration skills, eager to contribute and grow in a dynamic clinical research environment.