- Assisted Clinical Research Coordinators in various study-related duties, including organizing and filling study source documents, maintaining study binders, arching documents, and entering data from case report forms (CRFs) accurately and in timely manner.- Prepared and maintained study-relates source documents, ensuring accuracy and completeness, and creating study-specific forms both in paper and electronic formats. - Conducted detailed reviews of source documents prepared by Research Assistants, including Study Source document Templates (SSDTs) and Case Report Forms (CRFs), to ensure adherence to protocol and regulatory requirements. - Maintained thorough, accurate, and legible records to ensure compliance with regulatory standards and protocols. - Executed assigned tasks within the clinic, ensuring accuracy, timeliness, and organization in accordance with study protocols, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements. - Collaborated with Clinical Research Coordinator and BPSI Medical Writing groups to maintain regulatory binders. - Coordinated with Project Management and Data Management teams to achieve project-specific milestones and timelines. - Ensured the quality of scanned documents for data entry purposes, maintaining standards for accuracy and completeness. - Facilitated study monitor visits by coordinating with Clinical Research Coordinator, Project Management, and affected departments, ensuring all monitor/client expectations were met or exceeded. - Actively participated in clinical meetings and training session as required to stay updated on protocols and procedures. - Undertook other clinic-related tasks as assigned and as appropriate based on training and experience.