-Plan clinical trials in statistical perspective and write statistical methods section of protocols, statistical analysis plans and regulatory documents as needed forPhase I-IV clinical trials -Perform statistical analyses with multiple programming languages for clinical trials -Report statistical outcomes including tables, figures and listings for study reports, presentation and interpretation of results -Communicate results and data-specific issues to other team members -Collaborate with other team members such as Clinical Development and Regulatory Affairs; participating in various project towards achieving company objectives -Follow processes and adhere to Samsung and project specific standards as well as Health Authority requirements (SOP''s, Statistical Analysis Plan,GCP and regulatory guidelines) -Manage Contracted Research Organization (CRO) in biostatistics activities -Establish and maintain sound working relationships and effective communication within the biostatistics and data managementas well as with other business area