• Bachelor’s degree or Master degree in Biostatistics, Applied Statistics, or other related
• Minimum 3-year experience as a statistician in clinical trial or medical research
• Experience in team coordination
• Good writing and speaking in English language.
• Excellent conduct STATA software (others statistical software such as SAS, SPSS will be advantage)
• Regulatory requirements for clinical trials and medical research
• Ability to see the big picture, whilst still maintaining a focus on detail and implementation
• People with disabilities are encouraged to apply
Functional Competency
• Applied knowledge of advanced statistical models, such as generalized linear models, survival analyses and mixed models
• Data management skills for clinical trial and medical research
• Strong focus on quality and timely delivery of work
• Ability to work well and flexibly i.e. autonomously, in small teams and with a wide range of varying stakeholders
• Strong leadership and mentoring skills
• Excellent conduct STATA software (others statistical software such as SAS, SPSS will be advantage)