
HAO G.
CRA II @ InnoCare Pharma
About
CRA II, 3 yrs boots-on-the-ground across Phase I–III oncology, diabetes & rare disease. Fluent in the full site life-cycle—SSV, SIV, SMV, COV—juggling 16 parallel studies, 9 centres, zero major findings. Risk-based monitoring, bullet-proof GCP, contract negotiator, always road-ready: 75 % travel, same-day site-to-site jumps.
United States
Dallas
Pharmaceuticals
Pharmaceutical Industry, Protocol, Clinical Trials, GCP, Cell, Mac OS, Windows, GCP Certified, Teamwork, Microsoft PowerPoint, Laboratory Skills, Clinical Trials Monitoring Visit, source data verify(SDV), Microsoft Excel, Microsoft Office, Public Speaking, Healthcare, Clinical Research, 临床研究经验, 临床研究助理
Experience

CRA II
中国 广东省 广州
1.Completed center survey, SSU, SIV, routine inspection, data cleaning and center closure in accordance with GCP and company SOP 2.Checked the completeness and logic of the original documents, followed the ALCOA+CCEA principle for SDR and SDV work 3.Timely detect deviations and potential risks, and adopt effective CAPA 4.Multi-threaded work management 5.According to the sponsor's SOP and regulations, visit researchers regularly after completing the inspection,and write the inspection visit report and communication letter 6.Responsible for communication and coordination among researchers, SMO, sponsors and institutional ethics

CRA I
中国 广东省
1.Completed center survey, SSU, SIV, routine inspection, data cleaning and center closure in accordance with GCP and company SOP 2.Checked the completeness and logic of the original documents, followed the ALCOA+CCEA principle for SDR and SDV work 3.Timely detect deviations and potential risks, and adopt effective CAPA 4.Multi-threaded work management 5.According to the sponsor's SOP and regulations, visit researchers regularly after completing the inspection,and write the inspection visit report and communication letter 6.Responsible for communication and coordination among researchers, SMO, sponsors and institutional ethics
HAO G.'s Contact Information
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