Hanna Gang

- Conducting a systematic review & meta-analysis using real world data in hematological disease - Supported medical writing, making medical poster about ongoing observational study for Congress - According to the protocol, performed an internal e-CRF monitoring of ongoing observational study

- Standardized the clinical data from different databases and formulating according to the internal guidelines - Involved in managing data catalog system and integrating metadata for easy data asset discovery - Supported computational biology project : Simplified the protein-network visualization process through the R programming

Dedicated CTA - Medical department /Oncology team - IRB submission tasks include Amendment, Deviation, CSR - In charge of reporting safety mails (SUSAR case review, CIOMS review ) to study sites - Quality Control of e-TMF/s-TMF - Prepares, distributes, files, and archives clinical documentation Reviews study files periodically

Department of Pharmacology - Assist with early-phased trials (Phase I-II) under tight timeline. - Screening subjects following protocols and inclusion/exclusion criterias - Internal QC before monitor's visit as well as SDV experience in IIT study. - Review protocols and CRF, prepare Initiation meeting - Knowledge of ICH-GCP guideline

UMT(Local CRO) - Assisted clinical team and CRA with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines - Organized clinical master file documents and other supplements in multi-center clinical trials - Acted as a central contact for the clinical team for designated project communications

- Study design - Data analysis - SAS

Certified Medical coder - Medical informatics - Cancer registration - Pahthology - Medical Terminology