A day started with logging computer on and emails checking, followed by meeting with manager and with SAS programmer, discussing and prioritizing work. Some time met with data management team to communicate and support each other's need.
Worked on own tasks: statistical related works including supporting protocol developing, writing statistical analysis plan, conducting data review and surveillance, performing statistical analyses, creating results tables and listing, supporting medical writer with clinical study report(CSR), writing method section in CSR, and review CSR. Communicated with internal, and external team, if collaborated with CROs, by meetings, teleconferences (TC) and emails.
Working on different therapeutic area, built up knowledge and learned the different settings of different trials. And working on different phases of trials, built up knowledge in research and development of medications.